# FDA Inspection 912065 - Sedatelec - January 15, 2015

Source: https://www.keypedia.com/records/fda_inspections/sedatelec/2c555aa1-a5e7-40a1-b384-48b97b5284cf
Source feed: FDA_Inspections

> FDA Inspection 912065 for Sedatelec on January 15, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 912065
- Company Name: Sedatelec
- Inspection Date: 2015-01-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 912065 - 2015-01-15](https://www.keypedia.com/records/fda_inspections/sedatelec/e81aff38-c200-4704-b644-d66e45199388)
- [FDA Inspection 803691 - 2012-09-27](https://www.keypedia.com/records/fda_inspections/sedatelec/8e918ee0-3c0f-4a72-bf36-d8b6afd21d3a)
- [FDA Inspection 547246 - 2008-10-17](https://www.keypedia.com/records/fda_inspections/sedatelec/83bb6c69-6748-4491-afd8-2c132d6c2987)

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