FDA Warning Letter — Unipack LLC

Case 573233 — FEI 3008275696

The FDA took a Warning Letter action against Unipack LLC on June 6, 2019 (South Plainfield, NJ). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Unipack LLC
Date
June 6, 2019
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
South Plainfield, NJ (United States)