FDA Inspection 1274953 — LiquidCapsule Manufacturing, LLC
The FDA completed an inspection of LiquidCapsule Manufacturing, LLC on Jul 3, 2025 in Tampa, FL. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). 6 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Official Action Indicated (OAI)
- End Date
- Jul 3, 2025
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Tampa, FL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1105 | 21 CFR 211.22(d) | Procedures not in writing, fully followed |
| 1220 | 21 CFR 211.67(b)(3) | Cleaning SOPs/instructions |
| 1361 | 21 CFR 211.100(a) | Absence of Written Procedures |
| 1833 | 21 CFR 211.84(d)(1) | Identity Testing of Each Component |
| 1926 | 21 CFR 211.166(b) | Adequate number of batches on stability |
| 2012 | 21 CFR 211.188(b) | Batch production and Batch Control Record Requirements |