FDA Warning Letter — LiquidCapsule Manufacturing, LLC

Case 717069 — FEI 3006676534

The FDA took a Warning Letter action against LiquidCapsule Manufacturing, LLC on Dec 19, 2025 (Tampa, FL). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
LiquidCapsule Manufacturing, LLC
Date
Dec 19, 2025
Fiscal Year
2026
Product Type
Drugs
Center
CDER
Location
Tampa, FL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.