FDA Inspection 779611 — AMANN GIRRBACH AG

AMANN GIRRBACH AG — FEI 3006206552

The FDA completed an inspection of AMANN GIRRBACH AG on Apr 5, 2012 in Koblach. 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
Apr 5, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Koblach (Austria)

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