FDA Warning Letter — Keystone Laboratories, Inc.
The FDA took a Warning Letter action against Keystone Laboratories, Inc. on March 18, 2013 (Memphis, TN). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Keystone Laboratories, Inc.
- Date
- March 18, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Center
- CDER
- Location
- Memphis, TN (United States)