FDA Inspection 653387 — NIDEK Co., Ltd.

NIDEK Co., Ltd. — FEI 3002807715

The FDA completed an inspection of NIDEK Co., Ltd. on Feb 18, 2010 in Gamagoori. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Feb 18, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Gamagoori (Japan)

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