# FDA Inspection 1219420 - Synovo Production - October 02, 2023

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

> FDA Inspection 1219420 for Synovo Production on October 02, 2023. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1219420
- Company Name: Synovo Production
- Inspection Date: 2023-10-02
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276066 - 2025-06-12](https://www.keypedia.com/records/fda_inspections/synovo-production/65d5c9de-5041-4755-83a1-5c6643e500c8)
- [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)

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