# FDA Inspection 1062324 - DKK Dai-Ichi Shomei Co., Ltd. - July 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 for DKK Dai-Ichi Shomei Co., Ltd. on July 20, 2018. Classification: Official Action Indicated (OAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1062324 - 2018-07-20](https://www.keypedia.com/records/fda_inspections/dkk-dai-ichi-shomei-co-ltd/81bedf5b-9663-454e-97c8-3d9f049a689c)
- [FDA Inspection 879170 - 2014-05-01](https://www.keypedia.com/records/fda_inspections/dkk-dai-ichi-shomei-co-ltd/ff683c6a-c2cc-4373-a2b8-d30552366c95)

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