# 3M Unitek Corporation – FDA Inspection, Mar 27, 2014

Source: https://www.keypedia.com/records/fda_inspections/3m-unitek-corporation/f9a2c034-a20c-4a46-b4b7-7bb83aa86692
Source feed: FDA_Inspections

> FDA inspection 871900 of 3M Unitek Corporation, March 27, 2014. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 871900
- Company Name: 3M Unitek Corporation
- Inspection Date: 2014-03-27
- 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: 7

Company: https://www.keypedia.com/companies/3m-unitek-corporation/cd1571c6-eefa-4ff7-b8b3-abd4c68bc931

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