FDA Inspection
MSK Precision Products, Inc.MSK Precision Products, Inc. – FDA Inspection, Mar 21, 2017
Record Details
This FDA Inspection record concerns MSK Precision Products, Inc., with an inspection on March 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Paul A. Licata (Issuing Officer)
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ID · ff9afdd7-777e-4aa9-8aa6-db4c45fabe59
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1028776
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.198(a)Complaints
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of MSK Precision Products, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 17, 2025 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 14, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for MSK Precision Products, Inc.
- FDA Inspection 1288338 - 2025-10-17
- FDA Inspection 1210398 - 2023-07-14
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