# FDA Inspection 1260205 - Tung Keng Enterprise Co., Ltd. - January 09, 2025

Source: https://www.keypedia.com/records/fda_inspections/tung-keng-enterprise-co-ltd/8356ddab-c21e-4e8f-9e8e-bb8335fab4d3
Source feed: FDA_Inspections

> FDA Inspection 1260205 for Tung Keng Enterprise Co., Ltd. on January 09, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1260205
- Company Name: Tung Keng Enterprise Co., Ltd.
- Inspection Date: 2025-01-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1260205 - 2025-01-09](https://www.keypedia.com/records/fda_inspections/tung-keng-enterprise-co-ltd/cd3d0d6e-4e51-4496-a5f6-13cc39ea916e)
- [FDA Inspection 1260205 - 2025-01-09](https://www.keypedia.com/records/fda_inspections/tung-keng-enterprise-co-ltd/721a6214-f494-4806-9b76-9f493431cf6e)

Company: https://www.keypedia.com/companies/tung-keng-enterprise-co-ltd/ff8ca5d9-e041-41d0-bbf4-bceb0ae8d6ef

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