FDA Inspection
NIDEK Co., Ltd.NIDEK Co., Ltd. – FDA Inspection, Dec 8, 2017
Record Details
This FDA Inspection record concerns NIDEK Co., Ltd., with an inspection on December 8, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- NIDEK Co., Ltd.
- Inspection Date
- December 8, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 97815176-e2d2-4d5d-b986-ce4940be00d7
Inspection Facts
- Inspection number
- 1079761
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of NIDEK Co., Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| September 14, 2018 | Not classified | Office of Inspections and Investigations | |
| June 1, 2017 | Not classified | Office of Inspections and Investigations | Project Evaluation: Devices |
| July 31, 2014 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 18, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for NIDEK Co., Ltd.
- FDA Inspection 1132031 - 2018-09-14
- FDA Inspection 1013281 - 2017-06-01
- FDA Inspection 890755 - 2014-07-31
- FDA Inspection 653387 - 2010-02-18
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