# FDA Inspection 1099707 - Beijing Aeonmed Company Limited - July 18, 2019

Source: https://www.keypedia.com/records/fda_inspections/beijing-aeonmed-company-limited/a6d818fd-ef54-4af2-b0c3-c2e687d5c595
Source feed: FDA_Inspections

> FDA Inspection 1099707 for Beijing Aeonmed Company Limited on July 18, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099707
- Company Name: Beijing Aeonmed Company Limited
- Inspection Date: 2019-07-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1099707 - 2019-07-18](https://www.keypedia.com/records/fda_inspections/beijing-aeonmed-company-limited/4ffc4f17-05d5-4bbb-bd6c-a1846013b597)

Company: https://www.keypedia.com/companies/beijing-aeonmed-company-limited/aa5a5768-68eb-4901-bf20-bf64a508d50c

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