FDA Inspection 814591 — AMF, Sarl

AMF, Sarl — FEI 3004915132

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.