# MHC Medical Products LLC – FDA Inspection, Feb 2, 2018

Source: https://www.keypedia.com/records/fda_inspections/mhc-medical-products-llc/974d2f33-6adb-4230-98eb-92dde7fe399d
Source feed: FDA_Inspections

> FDA inspection 1039812 of MHC Medical Products LLC, February 02, 2018. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1039812
- Company Name: MHC Medical Products LLC
- Inspection Date: 2018-02-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1262263 - 2025-02-26](https://www.keypedia.com/records/fda_inspections/mhc-medical-products-llc/ede21849-e2fe-4634-8169-8aca7e7e0ee6)
- FDA Inspection 1180189 - 2022-09-23

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/christina-l-bigham/f3da8e26-4a8c-43a8-8070-349fe4500289)

Company: https://www.keypedia.com/companies/mhc-medical-products-llc/b5427535-3cbf-4ea5-9811-b7ee07feb7a3

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