# FDA Inspection 1241642 - Denka Co. Ltd. - May 23, 2024

Source: https://www.keypedia.com/records/fda_inspections/denka-co-ltd/2a9810dc-e450-4373-833b-117dc0cd94b4
Source feed: FDA_Inspections

> FDA Inspection 1241642 for Denka Co. Ltd. on May 23, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1241642
- Company Name: Denka Co. Ltd.
- Inspection Date: 2024-05-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1241642 - 2024-05-23](https://www.keypedia.com/records/fda_inspections/denka-co-ltd/1dc3f2c8-62e9-4bcd-ae3a-7d5c49025f43)
- [FDA Inspection 1022352 - 2017-07-06](https://www.keypedia.com/records/fda_inspections/denka-co-ltd/92f152f2-65f4-440b-91b2-ef347d4cdd69)

Company: https://www.keypedia.com/companies/denka-co-ltd/2a37bc8b-6daa-40d8-a78f-2f2a6a419c40

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