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FDA Inspection
•Osseolink USA, LLC•June 18, 2019

Osseolink USA, LLC – FDA Inspection, Jun 18, 2019

Record Details

This FDA Inspection record concerns Osseolink USA, LLC, with an inspection on June 18, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Osseolink USA, LLC
Inspection Date
June 18, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Brian S. Keefer (FDA Associated Person)
View Company Profile

ID · 0f9c391b-d8a8-42b1-aed7-31c1fe7fa94d

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1099236
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Osseolink USA, LLC

5
DateClassificationOfficeProject area
June 10, 2021NAICenter for Devices and Radiological HealthCompliance: Devices
June 25, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
January 29, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 19, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 8, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Osseolink USA, LLC
  • FDA Inspection 1145622 - 2021-06-10
  • FDA Inspection 884639 - 2014-06-25
  • FDA Inspection 863826 - 2014-01-29
  • FDA Inspection 764359 - 2012-01-19
  • FDA Inspection 640016 - 2010-01-08

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