FDA Warning Letter — Oculo Plastik, Inc.

Case 481113 — FEI 3002513507

The FDA took a Warning Letter action against Oculo Plastik, Inc. on December 22, 2015 (Montreal, Canada). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Oculo Plastik, Inc.
Date
December 22, 2015
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Montreal (Canada)