# FDA Inspection 783917 - Asahi Kasei Medical  MT Co.,  Okatomi Plant - May 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/asahi-kasei-medical-mt-co-okatomi-plant/2d837331-759f-4e99-be4d-bebf49948f7d
Source feed: FDA_Inspections

> FDA Inspection 783917 for Asahi Kasei Medical  MT Co.,  Okatomi Plant on May 23, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 783917
- Company Name: Asahi Kasei Medical  MT Co.,  Okatomi Plant
- Inspection Date: 2012-05-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 974282 - 2016-03-25](https://www.keypedia.com/records/fda_inspections/asahi-kasei-medical-mt-co-okatomi-plant/9a30d3e5-3634-4204-941f-bd7ee9227126)
- [FDA Inspection 783917 - 2012-05-23](https://www.keypedia.com/records/fda_inspections/asahi-kasei-medical-mt-co-okatomi-plant/93263565-a853-4a05-ae8a-6a4e8617c35c)

Company: https://www.keypedia.com/companies/asahi-kasei-medical-mt-co-okatomi-plant/084cdbb8-7129-4249-9a79-3df120b7b781

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