# FDA Inspection 937073 - Okamoto Industries, Inc. - July 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/okamoto-industries-inc/14fdfc7c-fa2b-4aba-bfe2-ef306ac5b915
Source feed: FDA_Inspections

> FDA Inspection 937073 for Okamoto Industries, Inc. on July 23, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 937073
- Company Name: Okamoto Industries, Inc.
- Inspection Date: 2015-07-23
- 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 937073 - 2015-07-23](https://www.keypedia.com/records/fda_inspections/okamoto-industries-inc/e901a1db-3d8c-4612-bf41-a916ef0f3f0b)

Company: https://www.keypedia.com/companies/okamoto-industries-inc/398388ea-77dd-4a73-b525-a7a3a0590996

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