FDA Inspection 988487 — Asap Endoscopic Products GmbH

Asap Endoscopic Products GmbH — FEI 3008494403

The FDA completed an inspection of Asap Endoscopic Products GmbH on Jul 8, 2016 in Umkirch. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 8, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Umkirch (Germany)

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