# FDA Inspection 871900 - 3M Unitek Corporation - March 27, 2014

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

> FDA Inspection 871900 for 3M Unitek Corporation on March 27, 2014. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 871900 - 2014-03-27](https://www.globalkeysolutions.net/api/records/fda_inspections/3m-unitek-corporation/25795856-63ce-49d2-863c-45993a98ace1/)

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

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