FDA Inspection 1009804 — B. Braun Melsungen AG

B. Braun Melsungen AG — FEI 3002806469

The FDA completed an inspection of B. Braun Melsungen AG on Mar 16, 2017 in Melsungen. 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
Mar 16, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Melsungen (Germany)

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