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FDA Inspection
•Gulf Fiberoptics, Inc.•March 23, 2023

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

Record Details

This FDA Inspection record concerns Gulf Fiberoptics, Inc., with an inspection on March 23, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Gulf Fiberoptics, Inc.
Inspection Date
March 23, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Monica C. Burgos Garcia
View Company Profile

ID · d15b4aa1-5a0a-4a45-8027-83f2ed627ffa

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1200561
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

Other FDA inspections of Gulf Fiberoptics, Inc.

7
DateClassificationOfficeProject area
December 18, 2019NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
August 13, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 6, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
February 3, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
May 3, 2011OAICenter for Devices and Radiological HealthCompliance: Devices
View all 7 other inspections on the company page
Other documents for Gulf Fiberoptics, Inc.
  • FDA Inspection 1114389 - 2019-12-18
  • FDA Inspection 938165 - 2015-08-13
  • FDA Inspection 830326 - 2013-05-06
  • FDA Inspection 766713 - 2012-02-03
  • FDA Inspection 722292 - 2011-05-03

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