# FDA Inspection 996125 - Okamoto Rubber Products Co., Ltd. - December 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/okamoto-rubber-products-co-ltd/6b6e8ff9-00b6-461e-a7ae-e9ffce769a34
Source feed: FDA_Inspections

> FDA Inspection 996125 for Okamoto Rubber Products Co., Ltd. on December 22, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 996125
- Company Name: Okamoto Rubber Products Co., Ltd.
- Inspection Date: 2016-12-22
- 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 996125 - 2016-12-22](https://www.keypedia.com/records/fda_inspections/okamoto-rubber-products-co-ltd/b7172434-cb4a-42b9-9e22-86026605db7c)
- [FDA Inspection 749471 - 2011-09-29](https://www.keypedia.com/records/fda_inspections/okamoto-rubber-products-co-ltd/0ea69645-71fe-41ee-9d99-ee0ff1db29de)
- [FDA Inspection 749471 - 2011-09-29](https://www.keypedia.com/records/fda_inspections/okamoto-rubber-products-co-ltd/0d6fa436-6564-4060-8fc1-a136522066e1)

Company: https://www.keypedia.com/companies/okamoto-rubber-products-co-ltd/1f149cc4-31ce-424d-ada7-69d93b229d7d

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