# FDA Inspection 850292 - Stille AB - August 22, 2013

Source: https://www.keypedia.com/records/fda_inspections/stille-ab/706f5fbd-248c-490e-bff8-aeb926da35a9
Source feed: FDA_Inspections

> FDA Inspection 850292 for Stille AB on August 22, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 850292
- Company Name: Stille AB
- Inspection Date: 2013-08-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/stille-ab/2f16f0d5-ab12-444a-a3aa-8ca22de10c71

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