FDA Inspection 1035853 — Hager & Meisinger Gmbh

Hager & Meisinger Gmbh — FEI 3004169071

The FDA completed an inspection of Hager & Meisinger Gmbh on Sep 7, 2017 in Neuss. 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
Sep 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Neuss (Germany)

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