FDA Inspection
Iridex CorporationIridex Corporation – FDA Inspection, Aug 8, 2019
Record Details
This FDA Inspection record concerns Iridex Corporation, with an inspection on August 8, 2019, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- Iridex Corporation
- Inspection Date
- August 8, 2019
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · e42a6ad6-fa89-4e3c-8e38-bfb36ad7ea6e
Inspection Facts
- Inspection number
- 1123978
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Iridex Corporation
6| Date | Classification | Office | Project area |
|---|---|---|---|
| September 20, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 2, 2023 | Not classified | San Francisco District Office | |
| August 19, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 2, 2014 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 10, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Iridex Corporation
- FDA Inspection 1218928 - 2023-09-20
- FDA Inspection 1201060 - 2023-03-02
- FDA Inspection 988542 - 2016-08-19
- FDA Inspection 906286 - 2014-12-02
- FDA Inspection 836353 - 2013-07-10
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