FDA Inspection 1052715 — OVESCO ENDOSCOPY AG

OVESCO ENDOSCOPY AG — FEI 3006696607

The FDA completed an inspection of OVESCO ENDOSCOPY AG on Jul 13, 2017 in Tubingen. 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
Jul 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Tubingen (Germany)

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