FDA Inspection 814591 — AMF, Sarl

AMF, Sarl — FEI 3004915132

The FDA completed an inspection of AMF, Sarl on December 6, 2012 in Lury Sur Arnon. 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
December 6, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Lury Sur Arnon (France)