# FDA Inspection 1200561 - Gulf Fiberoptics, Inc. - March 23, 2023

Source: https://www.keypedia.com/records/fda_inspections/gulf-fiberoptics-inc/a09cb7cd-a77d-4662-aa25-0c92bd0eb2fc
Source feed: FDA_Inspections

> FDA Inspection 1200561 for Gulf Fiberoptics, Inc. on March 23, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200561
- Company Name: Gulf Fiberoptics, Inc.
- Inspection Date: 2023-03-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1200561 - 2023-03-23](https://www.keypedia.com/records/fda_inspections/gulf-fiberoptics-inc/d15b4aa1-5a0a-4a45-8027-83f2ed627ffa)
- [FDA Inspection 1114389 - 2019-12-18](https://www.keypedia.com/records/fda_inspections/gulf-fiberoptics-inc/146579b1-75ad-4c37-8124-0aa69beb1b92)
- [FDA Inspection 1114389 - 2019-12-18](https://www.keypedia.com/records/fda_inspections/gulf-fiberoptics-inc/749b55d8-3977-4cb4-a1db-620d83896f27)
- [FDA Inspection 938165 - 2015-08-13](https://www.keypedia.com/records/fda_inspections/gulf-fiberoptics-inc/c892d0d4-0d86-4a43-8547-0dae1df49e74)
- [FDA Inspection 938165 - 2015-08-13](https://www.keypedia.com/records/fda_inspections/gulf-fiberoptics-inc/51742938-0eed-4870-8fa7-b72636445842)

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