FDA Inspection 1078121 — Nidek, Inc.
The FDA completed an inspection of Nidek, Inc. on January 24, 2019 in Fremont, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 24, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Fremont, CA (United States)