# FDA Inspection 1248487 - WEERO CO LTD - September 05, 2024

Source: https://www.keypedia.com/records/fda_inspections/weero-co-ltd/d059de5a-6dad-4e16-9c8a-4373e68d4f14
Source feed: FDA_Inspections

> FDA Inspection 1248487 for WEERO CO LTD on September 05, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1248487
- Company Name: WEERO CO LTD
- Inspection Date: 2024-09-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1248487 - 2024-09-05](https://www.keypedia.com/records/fda_inspections/weero-co-ltd/c60dcb84-1080-42e9-a90a-2ed850f1852b)

Company: https://www.keypedia.com/companies/weero-co-ltd/c9cc036a-c0b3-4245-898d-ef0172d8031b

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