# FDA Inspection 1243900 - AI DE Diagnostic Co., Ltd - May 30, 2024

Source: https://www.keypedia.com/records/fda_inspections/ai-de-diagnostic-co-ltd/a9599845-84c4-4c70-8b12-fb408c43f262
Source feed: FDA_Inspections

> FDA Inspection 1243900 for AI DE Diagnostic Co., Ltd on May 30, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1243900
- Company Name: AI DE Diagnostic Co., Ltd
- Inspection Date: 2024-05-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 957166 - 2016-01-28](https://www.keypedia.com/records/fda_inspections/ai-de-diagnostic-co-ltd/a8ddd04a-7979-4128-9850-4e138d1226dc)

Company: https://www.keypedia.com/companies/ai-de-diagnostic-co-ltd/49665e98-babf-4271-a0a3-b36bcf0c385b

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