# Sedatelec – FDA Inspection, Sep 27, 2012

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

> FDA inspection 803691 of Sedatelec, September 27, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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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)
- 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: 1

## Related Documents

- [FDA Inspection 1052129 - 2017-11-27](https://www.keypedia.com/records/fda_inspections/sedatelec/0c719485-5108-498f-998b-53e3b91e1ee6)
- FDA Inspection 912065 - 2015-01-15
- FDA Inspection 547246 - 2008-10-17

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