# Denka Co. Ltd. – FDA Inspection, Jul 6, 2017

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

> FDA inspection 1022352 of Denka Co. Ltd., July 06, 2017. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1241642 - 2024-05-23

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brittani-n-franklin/1d5e9344-1145-42ff-a175-5541b565b15e)

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