# McGuff Company Inc. – FDA Inspection, Mar 9, 2022

Source: https://www.keypedia.com/records/fda_inspections/mcguff-company-inc/d6e902d1-3a64-4728-adb1-7b4b61cd65b1
Source feed: FDA_Inspections

> FDA inspection 1164092 of McGuff Company Inc., March 09, 2022. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1164092
- Company Name: McGuff Company Inc.
- Inspection Date: 2022-03-09
- 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: 1

## Related Documents

- FDA Inspection 1257899 - 2024-12-09
- [FDA Inspection 1014257 - 2017-06-15](https://www.keypedia.com/records/fda_inspections/mcguff-company-inc/424aecdc-bf1b-4de6-96b9-a2e72fe5d2d4)
- FDA Inspection 983223 - 2016-05-24

Company: https://www.keypedia.com/companies/mcguff-company-inc/0e7de712-3f66-4fea-8bfe-f851677e46a4

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