FDA Warning Letter — Nidek Medical Products Inc

Case 42638 — FEI 1039215

The FDA took a Warning Letter action against Nidek Medical Products Inc on January 20, 2009 (Birmingham, AL). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Nidek Medical Products Inc
Date
January 20, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Birmingham, AL (United States)