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FDA Inspection
•Musculoskeletal Transplant Foundation, Inc.•March 13, 2009

Musculoskeletal Transplant Foundation, Inc. – FDA Inspection, Mar 13, 2009

Record Details

This FDA Inspection record concerns Musculoskeletal Transplant Foundation, Inc., with an inspection on March 13, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Musculoskeletal Transplant Foundation, Inc.
Inspection Date
March 13, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · e03a2c76-6bf3-4e09-bff8-7b5fa4829f12

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
573583
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Musculoskeletal Transplant Foundation, Inc.

11
DateClassificationOfficeProject area
August 4, 2026Not classifiedNew Jersey District OfficeHuman Cellular, Tissue, and Gene Therapies
June 21, 2024NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
March 9, 2022NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 17, 2021VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 18, 2018VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 11 other inspections on the company page
Other documents for Musculoskeletal Transplant Foundation, Inc.
  • FDA Inspection 1329314 - 2026-08-04
  • FDA Inspection 1229385 - 2024-06-21
  • FDA Inspection 1166490 - 2022-03-09
  • FDA Inspection 1160012 - 2021-11-17
  • FDA Inspection 1038552 - 2018-01-18

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