FDA Inspection 779658 — AMANN GIRRBACH GmbH

AMANN GIRRBACH GmbH — FEI 3006206547

The FDA completed an inspection of AMANN GIRRBACH GmbH on Apr 12, 2012 in Pforzheim. 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 12, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Pforzheim (Germany)

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