FDA Warning Letter — Nidek, Inc.

Case 434750 — FEI 2936921

The FDA took a Warning Letter action against Nidek, Inc. on August 8, 2014 (Fremont, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Nidek, Inc.
Date
August 8, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Fremont, CA (United States)