FDA Inspection 633822 — ALM ORTHO INC
The FDA completed an inspection of ALM ORTHO INC on Dec 10, 2009 in Scarborough, ME. 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
- Dec 10, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Scarborough, ME (United States)