# FDA Inspection 1034026 - Dr. Japan Co., Ltd. - November 09, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/dr-japan-co-ltd/88231c69-d9dd-41b8-a150-321d41f6810b
Source feed: FDA_Inspections

> FDA Inspection 1034026 for Dr. Japan Co., Ltd. on November 09, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034026
- Company Name: Dr. Japan Co., Ltd.
- Inspection Date: 2017-11-09
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1034026 - 2017-11-09](https://www.globalkeysolutions.net/records/fda_inspections/dr-japan-co-ltd/b3f0e794-0863-4ed0-844f-29fe77aadea5)
- [FDA Inspection 933520 - 2015-06-28](https://www.globalkeysolutions.net/records/fda_inspections/dr-japan-co-ltd/bdb62ec9-2a5b-410c-9800-8207a9fc09e2)

Company: https://www.globalkeysolutions.net/companies/dr-japan-co-ltd/ec2953c4-806d-48c5-94b9-e0f0e65740d3

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