# Entrotech Life Sciences, Inc. – FDA Inspection, Aug 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/entrotech-life-sciences-inc/db10a2c7-cc9d-448a-89e0-3ae6dc59bd45
Source feed: FDA_Inspections

> FDA inspection 1062290 of Entrotech Life Sciences, Inc., August 15, 2018. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1062290
- Company Name: Entrotech Life Sciences, Inc.
- Inspection Date: 2018-08-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1242772 - 2024-07-01](https://www.keypedia.com/records/fda_inspections/entrotech-life-sciences-inc/d75f39c1-81bc-4c16-9b50-7fe1b117fc26)
- FDA Inspection 1028826 - 2017-10-04
- FDA Inspection 749797 - 2011-10-11

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/quynh-strandberg/9b582ae6-85f9-4163-8ce6-b179c5fd340e)

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