# MSK Precision Products, Inc. – FDA Inspection, Mar 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/msk-precision-products-inc/ff9afdd7-777e-4aa9-8aa6-db4c45fabe59
Source feed: FDA_Inspections

> FDA inspection 1028776 of MSK Precision Products, Inc., March 21, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028776
- Company Name: MSK Precision Products, Inc.
- Inspection Date: 2017-03-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1288338 - 2025-10-17
- [FDA Inspection 1210398 - 2023-07-14](https://www.keypedia.com/records/fda_inspections/msk-precision-products-inc/1ae4446e-8f83-4ae8-adeb-800e0c487b06)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/msk-precision-products-inc/66fd1152-e5e9-47f6-a42a-5df92d8e9045

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7