FDA Inspection 840345 — Voco GmbH

Voco GmbH — FEI 3002718942

The FDA completed an inspection of Voco GmbH on Jun 20, 2013 in Cuxhaven. 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
Jun 20, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Cuxhaven (Germany)

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