FDA Inspection 820366 — AMD Medicom Inc. (GRANBY PLANT)

AMD Medicom Inc. (GRANBY PLANT) — FEI 3000164103

The FDA completed an inspection of AMD Medicom Inc. (GRANBY PLANT) on February 14, 2013 in Granby. 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
February 14, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Granby (Canada)