FDA Inspection
Precision Optics Corporation, Inc.Precision Optics Corporation, Inc. – FDA Inspection, Mar 31, 2023
Record Details
This FDA Inspection record concerns Precision Optics Corporation, Inc., with an inspection on March 31, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · a541b020-5824-47df-b253-482206badc3e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1201925
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
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Other FDA inspections of Precision Optics Corporation, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 11, 2025 | NAI | New England District Office | Postmarket Assurance: Medical Devices |
| June 12, 2017 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| April 7, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 14, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 27, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Precision Optics Corporation, Inc.
- FDA Inspection 1282350 - 2025-09-11
- FDA Inspection 1017022 - 2017-06-12
- FDA Inspection 965433 - 2016-04-07
- FDA Inspection 807445 - 2012-11-14
- FDA Inspection 685684 - 2010-09-27
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