# STRATEC SE – FDA Inspection, Jun 6, 2013

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

> FDA inspection 840250 of STRATEC SE, June 06, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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- FDA Inspection 712776 - 2011-02-10

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

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