FDA Warning Letter — Guna Inc.

Case 542995 — FEI 3007894121

The FDA took a Warning Letter action against Guna Inc. on January 11, 2018 (Whitehall, PA). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Guna Inc.
Date
January 11, 2018
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Whitehall, PA (United States)