# FDA Inspection 795185 - Stratec Switzerland AG - July 26, 2012

Source: https://www.keypedia.com/records/fda_inspections/stratec-switzerland-ag/373e1edb-9752-4432-9b6f-1e4c48a973dc
Source feed: FDA_Inspections

> FDA Inspection 795185 for Stratec Switzerland AG on July 26, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 795185
- Company Name: Stratec Switzerland AG
- Inspection Date: 2012-07-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 876144 - 2014-03-27](https://www.keypedia.com/records/fda_inspections/stratec-switzerland-ag/6d599af4-414c-4a8b-ad1d-45a089d23551)

Company: https://www.keypedia.com/companies/stratec-switzerland-ag/d3021696-6925-4474-b23a-a928f0b9208c

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