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FDA Inspection
•Oscor Caribe, LLC•January 18, 2023

Oscor Caribe, LLC – FDA Inspection, Jan 18, 2023

Record Details

This FDA Inspection record concerns Oscor Caribe, LLC, with an inspection on January 18, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Oscor Caribe, LLC
Inspection Date
January 18, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Adaliz Santaliz-Cruz (FDA Associated Person)
View Company Profile

ID · 100cb006-2524-4131-a791-ec656bc65fef

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1199358
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Oscor Caribe, LLC

5
DateClassificationOfficeProject area
August 22, 2025NAICompliance: Devices
December 11, 2019NAICenter for Devices and Radiological HealthCompliance: Devices
July 25, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
August 19, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
June 25, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Oscor Caribe, LLC
  • FDA Inspection 1300732 - 2025-08-22
  • FDA Inspection 1114423 - 2019-12-11
  • FDA Inspection 841836 - 2013-07-25
  • FDA Inspection 749326 - 2011-08-19
  • FDA Inspection 594560 - 2009-06-25

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