FDA Warning Letter — Novastep

Case 499206 — FEI 3010673777

The FDA took a Warning Letter action against Novastep on July 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
July 28, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Rennes (France)