# FDA Inspection 695885 - Sanjenics, Inc. - October 07, 2010

Source: https://www.keypedia.com/records/fda_inspections/sanjenics-inc/159dadb5-09d2-4a43-adb4-7ae8d10fc05d
Source feed: FDA_Inspections

> FDA Inspection 695885 for Sanjenics, Inc. on October 07, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 695885
- Company Name: Sanjenics, Inc.
- Inspection Date: 2010-10-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 695885 - 2010-10-07](https://www.keypedia.com/records/fda_inspections/sanjenics-inc/a0a8b056-edae-46f8-8fae-fe6476e136ef)

Company: https://www.keypedia.com/companies/sanjenics-inc/a02f89d4-a502-4c6f-b15b-1efefde0f7e0

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