FDA Inspection 1059140 — Microvapor Devices LLC
The FDA completed an inspection of Microvapor Devices LLC on July 17, 2018 in West Columbia, SC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 17, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- West Columbia, SC (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3232 | 21 CFR 820.72(a) | Equipment suitability & capability |
| 3235 | 21 CFR 820.72(a) | Equipment control activity documentation |