# DKK Dai-Ichi Shomei Co., Ltd. – FDA Inspection, Jul 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/dkk-dai-ichi-shomei-co-ltd/89d15e35-8cb6-43ec-bb66-8a48a11bc54a
Source feed: FDA_Inspections

> FDA inspection 1062324 of DKK Dai-Ichi Shomei Co., Ltd., July 20, 2018. Classification: Official Action Indicated (OAI). 7 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1062324
- Company Name: DKK Dai-Ichi Shomei Co., Ltd.
- Inspection Date: 2018-07-20
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- [FDA Inspection 879170 - 2014-05-01](https://www.keypedia.com/records/fda_inspections/dkk-dai-ichi-shomei-co-ltd/ff683c6a-c2cc-4373-a2b8-d30552366c95)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

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