# Synovo Production – FDA Inspection, Oct 2, 2023

Source: https://www.keypedia.com/records/fda_inspections/synovo-production/7940e37a-4fb5-4ef6-8756-68944bede375
Source feed: FDA_Inspections

> FDA inspection 1219420 of Synovo Production, October 02, 2023. Classification: Official Action Indicated (OAI). 8 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: 1219420
- Company Name: Synovo Production
- Inspection Date: 2023-10-02
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- [FDA Inspection 1276066 - 2025-06-12](https://www.keypedia.com/records/fda_inspections/synovo-production/6adae857-3382-40f8-af80-f1bc1296c80c)
- [FDA Inspection 1182099 - 2022-10-26](https://www.keypedia.com/records/fda_inspections/synovo-production/a95306b1-a21c-4860-8bba-3734329ddd3d)

## Related Officers

- [Investigator](https://www.keypedia.com/people/kevin-n-tran/dd74120c-4a8d-4fd0-9068-c862890d00d6)

Company: https://www.keypedia.com/companies/synovo-production/e55218cc-2f72-4106-8604-f7d9a0bc58d6

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