Question

In: Statistics and Probability

1 . The Food and Drug Administration has decided if a particular food product has 8...

1 . The Food and Drug Administration has decided if a particular food product has 8 grams or more of impurities it should be banned. A random sample of 36 cans of Tomato soup produced by Classic Food, Inc. showed 7.4 grams of impurities with a standard deviation of 3 grams. Test the hypothesis at the 1% level of significance. Please show the process of getting the answer

2. A production process is designed to fill cans with exactly 32 ounces of chicken noodle soup. A random sample of 49 cans was selected and inspected. The average weight of the cans in the sample is 31.9 ounces with a standard deviation of 0.5. Test the hypothesis at a 2% level of significance.  Please show the process of getting the answer

Solutions

Expert Solution

1 ) Given : Sample size=n=36

Sample mean=7.4

Sample standard deviation=s=3

Significance level=0.01

Population mean=8

Hypothesis:    VS

The test statistic under Ho is ,

Critical value : Since , the test is left tailed test

Decision : Here ,

Therefore , fail to reject Ho at 1% level of significance

Conclusion : Hence , there is sufficient evidence to conclude that the food and drug administration has decided the production should be banned.

2 ) Given : Sample size=n=49

Sample mean=31.9

Sample standard deviation=s=0.5

Significance level=0.02

Population mean=32

Hypothesis:    VS

The test statistic under Ho is ,

Critical value :

Decision : Here ,

Therefore , fail to reject Ho at 2% level of significance

Conclusion : Hence , there is sufficient evidence to conclude that the production process is designed to fill cans with exactly 32 ounces of chicken noodle soup


Related Solutions

The Food and Drug Administration will allow a food product to be labeled “sodium free” only...
The Food and Drug Administration will allow a food product to be labeled “sodium free” only if there is strong evidence that it contains, on average, less than 5 milligrams of sodium per serving. A soft drink producer, wishing to use a “salt free” label, has its product tested. A laboratory takes 25 independent sample servings of the soft drink and measures them for sodium content using a technique that is practically free of bias. These measurements average 4.9 milligrams...
The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug...
The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug should contain less than 25mg of the active ingredient “toxin”, which is assumed to have dangerous side effects. The FDA would like to restrict the error of “approving the drug despite its too high content of toxin” to a maximum risk of 5% (α ≤ 0.05). Let Xi : “ The content of toxin in the i-th pill [in mg].” ∼ N(µ, σ2 )...
A drug company applied for the approval of the Food and Drug Administration (FDA) to market...
A drug company applied for the approval of the Food and Drug Administration (FDA) to market a miracle drug that the company believed could cure some cancers. During the period that the application was under consideration the company's stock rose to $65 per share. The president of the company learned that the FDA application was about to be denied. You are a personal friend of the president, and he told you that he believed that the stock will start trading...
1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...
1. The The Food and Drug Administration (FDA) requires which ONE of the following products to contain specific levels of microbial inhibitors or acidifying agents such as phosphoric or citric acid to prevent production of Clostridium botulinum toxin in the product? (NOTE: An anaerobic environment is present in both bottled and canned products. ) Hint: Look at the lecture slides that discuss how some of these products are made. You can also look up specific information for these items on...
1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...
1. The The Food and Drug Administration (FDA) requires which ONE of the following products to contain specific levels of microbial inhibitors or acidifying agents such as phosphoric or citric acid to prevent production of Clostridium botulinum toxin in the product? (NOTE: An anaerobic environment is present in both bottled and canned products. ) Hint: Look at the lecture slides that discuss how some of these products are made. You can also look up specific information for these items on...
(20pts) The Food and Drug Administration (FDA) has established an upper tolerance of 5 parts per...
(20pts) The Food and Drug Administration (FDA) has established an upper tolerance of 5 parts per billion for the cancer-causing substance nitrosamine in beer. Suppose that Pabst and Miller are identified by the FDA as containing excessive concentrations of nitrosamines and are tested by an independent testing agency with the results shown in the accompanying table (in parts per billion). Also suppose that 36 bottles were randomly selected from each brand.                      Stat.     Pabst    Miller                      --------  -----    ------                      Mean      5.25     5.31                      Std. Dev. 1.20     1.44 Specify the null...
Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is...
Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is too easy and, as a result, too many drugs are approved that are later found to be pushed for a more lenient approval process so that pharmaceutical companies can get new drugs approved more easily and quickly. Consider a null hypothesis that a new, unapproved drug is unsafe and an alternative hypothesis that a new, unapproved drug is safe. Differentiate Type 1 and Type...
What is the U.S. Food and Drug Administration purity standard for medical O2?
What is the U.S. Food and Drug Administration purity standard for medical O2?95%21%90%99%
D. a) Discuss the functional differences between the Food and Drug Administration and the Center for...
D. a) Discuss the functional differences between the Food and Drug Administration and the Center for Medicare and Medicaid Services (see the web links below). b) Discuss how the two regulatory agencies influence your professional nursing practice. c)Describe your role as a patient advocate in promoting safety when a patient has requested to use an alternative therapy. d) Discuss the purposes of the Nurse Practice Act in your state and its impact on your professional practice. e) Discuss the scope...
The Food and Drug Administration (FDA) is an agency of the United States Department of Health...
The Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services, one of the United States' federal executive departments. The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, prescriptions, and other health-related products. The following are a few examples of the powers the FDA has: • Most federal laws concerning the FDA are part of the Food, Drug, and Cosmetic Act....
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT