FDA Inspection 813877 — The Flexite Company
The FDA completed an inspection of The Flexite Company on Jan 9, 2013 in Mineola, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jan 9, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Mineola, NY (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 636 | 21 CFR 803.17(b)(2) | Reports and information documentation |