FDA Warning Letter — Rainbow Gold Products Inc

Case 508837 — FEI 3002784388

The FDA took a Warning Letter action against Rainbow Gold Products Inc on May 4, 2017 (Sardis City, AL). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Rainbow Gold Products Inc
Date
May 4, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Sardis City, AL (United States)