FDA Inspection 914433 — Gb Implantat Technologie GMBH

Gb Implantat Technologie GMBH — FEI 3000258338

The FDA completed an inspection of Gb Implantat Technologie GMBH on Feb 11, 2015 in Bochum. 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
Feb 11, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Bochum (Germany)

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