FDA Inspection 755099 — ALM ORTHO INC

ALM ORTHO INC — FEI 3029890418

The FDA completed an inspection of ALM ORTHO INC on November 30, 2011 in Scarborough, ME. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 30, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Scarborough, ME (United States)