# FDA Inspection 991826 - Endotec, Inc. - October 14, 2016

Source: https://www.keypedia.com/records/fda_inspections/endotec-inc/390af2b5-a689-4e37-a17f-cab18ebb2dbb
Source feed: FDA_Inspections

> FDA Inspection 991826 for Endotec, Inc. on October 14, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991826
- Company Name: Endotec, Inc.
- Inspection Date: 2016-10-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 991826 - 2016-10-14](https://www.keypedia.com/records/fda_inspections/endotec-inc/54db0071-85db-4bf7-a3e6-3ce002d87dfb)
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Company: https://www.keypedia.com/companies/endotec-inc/db3ee6a3-e86b-4cb9-ab17-eeff33ebcfe5

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