# Deymed Diagnostic SRO – FDA Inspection, Jul 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/deymed-diagnostic-sro/d409bf38-ced7-4c10-9d2f-64663ed64389
Source feed: FDA_Inspections

> FDA inspection 1214862 of Deymed Diagnostic SRO, July 27, 2023. Classification: Official Action Indicated (OAI). 12 citations under 21 CFR parts 801, 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1214862
- Company Name: Deymed Diagnostic SRO
- Inspection Date: 2023-07-27
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

## Related Documents

- [FDA Inspection 1268057 - 2025-03-27](https://www.keypedia.com/records/fda_inspections/deymed-diagnostic-sro/71322fda-634e-42c2-a43f-f22b4a5d8e29)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

Company: https://www.keypedia.com/companies/deymed-diagnostic-sro/227737ad-7694-4077-a922-90210bb3ddec

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