FDA Inspection 637658 — Omni Management
The FDA completed an inspection of Omni Management on Jan 5, 2010 in Decatur, AL. 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
- Jan 5, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Decatur, AL (United States)