# Dr. Japan Co., Ltd. – FDA Inspection, Nov 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/dr-japan-co-ltd/b3f0e794-0863-4ed0-844f-29fe77aadea5
Source feed: FDA_Inspections

> FDA inspection 1034026 of Dr. Japan Co., Ltd., November 09, 2017. Classification: Official Action Indicated (OAI). Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- 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: 0

## Related Documents

- FDA Inspection 933520 - 2015-06-28

## Related Officers

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

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

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