# FDA Inspection 952580 - 3M Company - November 06, 2015

Source: https://www.keypedia.com/records/fda_inspections/3m-company/bebefe39-576b-4eb1-978b-38dfdd7a0405
Source feed: FDA_Inspections

> FDA Inspection 952580 for 3M Company on November 06, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 952580
- Company Name: 3M Company
- Inspection Date: 2015-11-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 716609 - 2011-03-29](https://www.keypedia.com/records/fda_inspections/3m-company/0a6bde45-127a-4415-99bd-9d974be61bc2)
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Company: https://www.keypedia.com/companies/3m-company/df9eaa46-6807-4afd-ab61-cfe32564eb0a

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