FDA Warning Letter — Best Bentonite

Case 494502 — FEI 3012095980

The FDA took a Warning Letter action against Best Bentonite on June 17, 2016 (Guthrie, OK). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Best Bentonite
Date
June 17, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
Guthrie, OK (United States)