FDA Warning Letter — Hybrid Pharma LLC

Case 566443 — FEI 3011319445

The FDA took a Warning Letter action against Hybrid Pharma LLC on November 30, 2018 (Deerfield Beach, FL). The action was issued by CDER and concerns drugs products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Hybrid Pharma LLC
Date
November 30, 2018
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Deerfield Beach, FL (United States)