# FDA Inspection 1264480 - Shenzhen Osto Medical Technology Co.,LTD - March 20, 2025

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-osto-medical-technology-coltd/76aacf1e-6b61-4daf-83a1-aeda3a997de9
Source feed: FDA_Inspections

> FDA Inspection 1264480 for Shenzhen Osto Medical Technology Co.,LTD on March 20, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1264480
- Company Name: Shenzhen Osto Medical Technology Co.,LTD
- Inspection Date: 2025-03-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1264480 - 2025-03-20](https://www.keypedia.com/records/fda_inspections/shenzhen-osto-medical-technology-coltd/34f0525f-4fdd-494e-bfaa-c6ad39fe81f9)

Company: https://www.keypedia.com/companies/shenzhen-osto-medical-technology-coltd/92e6ef0c-a142-4b35-a65c-4503913049a4

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