FDA Inspection
Nidek, Inc.Nidek, Inc. – FDA Inspection, Mar 31, 2017
Record Details
This FDA Inspection record concerns Nidek, Inc., with an inspection on March 31, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · f792cf22-b8f9-4fdd-a305-0bca1a1709d5
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1009390
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Nidek, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| January 24, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 10, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 10, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 14, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 30, 2013 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Nidek, Inc.
- FDA Inspection 1078121 - 2019-01-24
- FDA Inspection 980717 - 2016-08-10
- FDA Inspection 930830 - 2015-06-10
- FDA Inspection 871244 - 2014-04-14
- FDA Inspection 842321 - 2013-07-30
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