FDA Inspection 1263186 — Trividia Manufacturing Solutions, Inc.
The FDA completed an inspection of Trividia Manufacturing Solutions, Inc. on March 6, 2025 in Lancaster, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- March 6, 2025
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Lancaster, NH (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1111 | 21 CFR 211.25(a) | Training , Education , Experience overall |
| 2027 | 21 CFR 211.192 | Investigations of discrepancies, failures |
| 2399 | 21 CFR 211.194(a)(2) | Laboratory Test Method Verification |
| 2419 | 21 CFR 211.198(a) | Complaint Handling Procedure |