# FDA Inspection 1022352 - Denka Co. Ltd. - July 06, 2017

Source: https://www.keypedia.com/records/fda_inspections/denka-co-ltd/92f152f2-65f4-440b-91b2-ef347d4cdd69
Source feed: FDA_Inspections

> FDA Inspection 1022352 for Denka Co. Ltd. on July 06, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022352
- Company Name: Denka Co. Ltd.
- Inspection Date: 2017-07-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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