# Entrotech Life Sciences, Inc. – FDA Inspection, Jul 1, 2024

Source: https://www.keypedia.com/records/fda_inspections/entrotech-life-sciences-inc/d75f39c1-81bc-4c16-9b50-7fe1b117fc26
Source feed: FDA_Inspections

> FDA inspection 1242772 of Entrotech Life Sciences, Inc., July 01, 2024. Classification: Voluntary Action Indicated (VAI). 2 citations 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: 1242772
- Company Name: Entrotech Life Sciences, Inc.
- Inspection Date: 2024-07-01
- 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 1062290 - 2018-08-15](https://www.keypedia.com/records/fda_inspections/entrotech-life-sciences-inc/db10a2c7-cc9d-448a-89e0-3ae6dc59bd45)
- FDA Inspection 1028826 - 2017-10-04
- FDA Inspection 749797 - 2011-10-11

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

Company: https://www.keypedia.com/companies/entrotech-life-sciences-inc/ad58859b-753f-49f8-9fc8-37ed6f74a226

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