# DKK Dai-Ichi Shomei Co., Ltd. – FDA Inspection, May 1, 2014

Source: https://www.keypedia.com/records/fda_inspections/dkk-dai-ichi-shomei-co-ltd/ff683c6a-c2cc-4373-a2b8-d30552366c95
Source feed: FDA_Inspections

> FDA inspection 879170 of DKK Dai-Ichi Shomei Co., Ltd., May 01, 2014. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 879170
- Company Name: DKK Dai-Ichi Shomei Co., Ltd.
- Inspection Date: 2014-05-01
- 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: 0

## Related Documents

- [FDA Inspection 1062324 - 2018-07-20](https://www.keypedia.com/records/fda_inspections/dkk-dai-ichi-shomei-co-ltd/89d15e35-8cb6-43ec-bb66-8a48a11bc54a)

Company: https://www.keypedia.com/companies/dkk-dai-ichi-shomei-co-ltd/e58c568f-a6e8-4d82-a02f-1bd9cbcd66ab

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