Find Bonner County Idaho 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 Eastport 537896 U.s. 95 Bonners Ferry ID 83805 50.9 miles from Bonner County 208-267-7314
FDA Office of Regulatory Affairs Spokane 621 North Argonne Road Spokane Valley WA 99212 54.8 miles from Bonner County 509-353-2554
FDA Office of Regulatory Affairs Oroville 33643 U.s. 97 Oroville WA 98844 137.4 miles from Bonner County 509-476-3688
FDA Office of Regulatory Affairs Helena 10 West 15th Street Helena MT 59626 245.4 miles from Bonner County 406-441-1173
FDA Office of Regulatory Affairs Seattle District Office 22215 26th Avenue Southeast Bothell WA 98021 259.7 miles from Bonner County 425-302-0340
FDA Pacific Regional Laboratory Northwest 22201 23rd Drive Southeast Bothell WA 98021 259.9 miles from Bonner County 425-487-5300
FDA Office of Regulatory Affairs Puget Sound 1000 2nd Avenue Seattle WA 98104 268.6 miles from Bonner County 206-553-7001
FDA Office of Regulatory Affairs Tacoma 949 Market Street Tacoma WA 98402 279.8 miles from Bonner County 253-383-5252
FDA Office of Regulatory Affairs Blaine 9901 Pacific Highway Blaine WA 98230 282.6 miles from Bonner County 360-332-2646
FDA Office of Regulatory Affairs Boise 550 West Fort Street Boise ID 83724 325.6 miles from Bonner County 208-334-9012
FDA Office of Regulatory Affairs Portland Airport 7820 Northeast Holman Street Portland OR 97218 339.2 miles from Bonner County 503-262-8748
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.
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.
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.