FDA Inspection 541724 — The Flexite Company
The FDA completed an inspection of The Flexite Company on Oct 8, 2008 in Mineola, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Oct 8, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Mineola, NY (United States)