FDA Inspection 1063417 — Trividia Manufacturing Solutions, Inc.
The FDA completed an inspection of Trividia Manufacturing Solutions, Inc. on August 24, 2018 in Lancaster, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- August 24, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Lancaster, NH (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 4352 | 21 CFR 211.160(b)(4) | Calibration - at intervals, written program, remedial action |