# FDA Inspection 840250 - STRATEC SE - June 06, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/stratec-se/2f272b05-f8f0-4f3c-b05f-4080835a65bf
Source feed: FDA_Inspections

> FDA Inspection 840250 for STRATEC SE on June 06, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 840250
- Company Name: STRATEC SE
- Inspection Date: 2013-06-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/stratec-se/915e80d4-1029-4004-b683-1e09532124a8

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