FDA Inspection 804827 — F&L Medical Products Co
The FDA completed an inspection of F&L Medical Products Co on Oct 25, 2012 in Vandergrift, PA. 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 25, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Vandergrift, PA (United States)