FDA Inspection 1053177 — Alber GmbH

Alber GmbH — FEI 3004730072

The FDA completed an inspection of Alber GmbH on Apr 12, 2018 in Albstadt. 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, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Albstadt (Germany)

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