FDA Inspection
NIDEK Co., Ltd.NIDEK Co., Ltd. – FDA Inspection, Sep 14, 2018
Record Details
This FDA Inspection record concerns NIDEK Co., Ltd., with an inspection on September 14, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- NIDEK Co., Ltd.
- Inspection Date
- September 14, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · d8f907ed-241b-4f2e-bfc6-9dbe7f584c7f
Inspection Facts
- Inspection number
- 1132031
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of NIDEK Co., Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| December 8, 2017 | 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 1079761 - 2017-12-08
- FDA Inspection 1013281 - 2017-06-01
- FDA Inspection 890755 - 2014-07-31
- FDA Inspection 653387 - 2010-02-18
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