# Synedgen Inc. – FDA Inspection, Jul 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/synedgen-inc/d3da6f07-7c93-4062-b0e4-7111450d4c45
Source feed: FDA_Inspections

> FDA inspection 1097763 of Synedgen Inc., July 26, 2019. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097763
- Company Name: Synedgen Inc.
- Inspection Date: 2019-07-26
- 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: 2

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/angelica-g-aziz/3aea89c9-72d6-4865-984e-936dd61d2786)
- [Issuing Officer](https://www.keypedia.com/people/esteban-beltran/9a9bf6b2-ecdf-494c-82f4-5ef5932d629a)

Company: https://www.keypedia.com/companies/synedgen-inc/a1d04c3b-ea1c-4d03-a484-5cd727c38e34

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