FDA Inspection 734724 — MaxiFlex, LLC
The FDA completed an inspection of MaxiFlex, LLC on May 11, 2011 in New Orleans, LA. 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
- May 11, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Orleans, LA (United States)