# FDA Inspection 803691 - Sedatelec - September 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/sedatelec/8e918ee0-3c0f-4a72-bf36-d8b6afd21d3a
Source feed: FDA_Inspections

> FDA Inspection 803691 for Sedatelec on September 27, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803691
- Company Name: Sedatelec
- Inspection Date: 2012-09-27
- 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.keypedia.com/companies/sedatelec/745fa75a-b7e5-4d2f-8dc2-d44233eeb3f3

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