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FDA Inspection
•Osseolink USA, LLC•January 29, 2014

Osseolink USA, LLC – FDA Inspection, Jan 29, 2014

Record Details

This FDA Inspection record concerns Osseolink USA, LLC, with an inspection on January 29, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Osseolink USA, LLC
Inspection Date
January 29, 2014
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · c25f25be-fc5b-41db-9086-a8c82d1e0583

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
863826
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Osseolink USA, LLC

5
DateClassificationOfficeProject area
June 10, 2021NAICenter for Devices and Radiological HealthCompliance: Devices
June 18, 2019NAICenter for Devices and Radiological HealthCompliance: Devices
June 25, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
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 1099236 - 2019-06-18
  • FDA Inspection 884639 - 2014-06-25
  • FDA Inspection 764359 - 2012-01-19
  • FDA Inspection 640016 - 2010-01-08

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