11561 FDA

Find 11561 FDA offices, centers, labs and buildings of the US Food and Drug Administration. FDA offices provide information on food safety and recalls, drugs, pharmaceutical and medication approval, research, testing and regulation, medical devices, vaccines, cosmetics, tobacco products and regulatory science and consumer safety.


FDA Office of Regulatory Affairs New York District 158-15 Liberty Avenue Jamaica NY 11433 11.0 miles from 11561 718-340-7000


U.S. Food & Drug Administration Northeast Region New York 158-15 Liberty Avenue Jamaica NY 11433 11.0 miles from 11561 718-340-7000

U.S. Food & Drug Administration Northeast Regional Laboratory 158-15 Liberty Avenue Jamaica NY 11433 11.0 miles from 11561 718-662-5450

FDA Office Of Criminal Investigations - New York Field Office 10 Exchange Place Jersey NJ 07302 22.0 miles from 11561 201-547-3851

FDA Office of Regulatory Affairs Long Island 170 Federal Plaza Central Islip NY 11722 26.7 miles from 11561 613-787-3002

FDA Office of Regulatory Affairs Port Elizabeth 1201 Corbin Street Elizabeth NJ 07201 27.9 miles from 11561 908-527-2461

FDA Office of Regulatory Affairs White Plains 300 Hamilton Avenue White Plains NY 10601 31.4 miles from 11561 914-682-6166

FDA Office of Regulatory Affairs North Brunswick 629 Cranbury Road East Brunswick NJ 08816 42.6 miles from 11561 732-390-3800

FDA Office of Regulatory Affairs New Jersey District Office 10 Waterview Boulevard Parsippany-Troy Hills NJ 07054 45.2 miles from 11561 973-331-4900

FDA Office of Regulatory Affairs Bridgeport 915 Lafayette Boulevard Bridgeport CT 06604 46.9 miles from 11561 203-579-5822

If the FDA does not monitor meat, poultry, and egg products, who does?

The FDA is responsible for about 80% of the food consumed in the U.S. However, the FDA does not monitor meat, poultry, and egg products. The Food Safety Inspection Services of the U.S. Department of Agriculture is responsible for the safety, proper packaging, and labeling of meat, poultry, and egg products.

What is a recall?

A recall is when a product is removed from the market because it is defective, potentially harmful, or poses some safety threat. Recalls can either be voluntary on the part of the company or can be in response to action by the FDA.

Do over the counter medications follow the same approval process as prescription drugs?

No. For over the counter drugs, the FDA tests the active ingredients and labeling. Once the safety, effectiveness, and labeling of the active ingredient has been established, new products that comply with a set of standards for that active ingredient generally do not require new approval.