FDA Warning Letter — Novastep

Case 499206 — FEI 3010673777

The FDA took a Warning Letter action against Novastep on Jul 28, 2016 (Rennes, France). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action details

Facility
Novastep
Date
Jul 28, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Rennes (France)

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