# Endo-Therapeutics, Inc. – FDA Inspection, Feb 7, 2017

Source: https://www.keypedia.com/records/fda_inspections/endo-therapeutics-inc/e5c5caf9-825b-4579-a017-b19273f40af8
Source feed: FDA_Inspections

> FDA inspection 1000402 of Endo-Therapeutics, Inc., February 07, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000402
- Company Name: Endo-Therapeutics, Inc.
- Inspection Date: 2017-02-07
- 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: 2

## Related Documents

- [FDA Inspection 807443 - 2012-11-15](https://www.keypedia.com/records/fda_inspections/endo-therapeutics-inc/332e96db-b757-45fd-84dc-2d2842db830a)
- [FDA Inspection 544243 - 2008-10-22](https://www.keypedia.com/records/fda_inspections/endo-therapeutics-inc/33126fb5-216a-4d9f-a2e2-19f82e558fca)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/endo-therapeutics-inc/11feda6a-10da-427e-8937-c997fa90880b

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