# Gulf Fiberoptics, Inc. – FDA Inspection, Mar 23, 2023

Source: https://www.keypedia.com/records/fda_inspections/gulf-fiberoptics-inc/d15b4aa1-5a0a-4a45-8027-83f2ed627ffa
Source feed: FDA_Inspections

> FDA inspection 1200561 of Gulf Fiberoptics, Inc., March 23, 2023. Classification: No Action Indicated (NAI). Form 483 issued. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200561
- Company Name: Gulf Fiberoptics, Inc.
- Inspection Date: 2023-03-23
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1114389 - 2019-12-18
- FDA Inspection 938165 - 2015-08-13
- FDA Inspection 830326 - 2013-05-06
- [FDA Inspection 766713 - 2012-02-03](https://www.keypedia.com/records/fda_inspections/gulf-fiberoptics-inc/3446b968-3b31-43d8-9d8a-7b7b158687d4)
- [FDA Inspection 722292 - 2011-05-03](https://www.keypedia.com/records/fda_inspections/gulf-fiberoptics-inc/ffaeb1be-7a6f-4e6e-8582-f0417f9a283e)

## Related Officers

- [Monica C. Burgos Garcia](https://www.keypedia.com/people/monica-c-burgos-garcia/d73d6ad6-4158-4c12-a0bf-6f5721db3400)

Company: https://www.keypedia.com/companies/gulf-fiberoptics-inc/b6615066-b9af-4514-9ef1-203cc562deda

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7