# FDA Inspection 933588 - SUZUKEN CO., LTD. OGUCHI CENTER - June 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/suzuken-co-ltd-oguchi-center/9340aaad-1bad-4ec9-a204-e1a094bd0414
Source feed: FDA_Inspections

> FDA Inspection 933588 for SUZUKEN CO., LTD. OGUCHI CENTER on June 17, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 933588
- Company Name: SUZUKEN CO., LTD. OGUCHI CENTER
- Inspection Date: 2015-06-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 933588 - 2015-06-17](https://www.keypedia.com/records/fda_inspections/suzuken-co-ltd-oguchi-center/c68cb1fd-1cfa-4929-9efd-6f22f9efb720)
- [FDA Inspection 866643 - 2014-01-30](https://www.keypedia.com/records/fda_inspections/suzuken-co-ltd-oguchi-center/a654f6db-199e-49e1-b8cc-56bf392b7ce8)
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Company: https://www.keypedia.com/companies/suzuken-co-ltd-oguchi-center/58c75523-8ed0-42f5-b961-1e2cd84980d4

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