FDA Inspection
Musculoskeletal Transplant Foundation, Inc.Musculoskeletal Transplant Foundation, Inc. – FDA Inspection, Jul 30, 2010
Record Details
This FDA Inspection record concerns Musculoskeletal Transplant Foundation, Inc., with an inspection on July 30, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- July 30, 2010
- Product Type
- Biologics
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ID · e75eb64c-5efd-4dca-9b65-0f0df306099f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 674577
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
9- 21 CFR 1271.260(d)Corrective actions
- 21 CFR 1271.200(e)Documentation of maintenance and cleaning
- 21 CFR 1271.50(b)(1)Donor screening standards
- 21 CFR 1271.190(a)State of repair
- 21 CFR 1271.220(a)Causing contamination, increasing risks
- 21 CFR 1271.190(d)(1)Procedures for cleaning, sanitation
- 21 CFR 1271.250(a)Controlling the labeling of HCT/Ps
- 21 CFR 1271.260(a)Contamination, mix ups, improper release
- 21 CFR 1271.210(a)Use prior to verification
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Other FDA inspections of Musculoskeletal Transplant Foundation, Inc.
11| Date | Classification | Office | Project area |
|---|---|---|---|
| August 4, 2026 | Not classified | New Jersey District Office | Human Cellular, Tissue, and Gene Therapies |
| June 21, 2024 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 9, 2022 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 17, 2021 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 18, 2018 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
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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