FDA Inspection 851813 — NEWCLIP TECHNICS SAS

NEWCLIP TECHNICS SAS — FEI 3007143290

The FDA completed an inspection of NEWCLIP TECHNICS SAS on Sep 14, 2013 in Haute-Goulaine. 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
Sep 14, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Haute-Goulaine (France)

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