FDA Warning Letter — NIDEK Co., Ltd.

Case 410944 — FEI 3002807715

The FDA took a Warning Letter action against NIDEK Co., Ltd. on Sep 24, 2013 (Gamagoori, Japan). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action details

Facility
NIDEK Co., Ltd.
Date
Sep 24, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Gamagoori (Japan)

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