# FDA Inspection 750738 - Asahi Roentgen Ind. Co., Ltd - September 15, 2011

Source: https://www.keypedia.com/records/fda_inspections/asahi-roentgen-ind-co-ltd/3e0738a0-1dd1-4b8b-98fc-8a80aedb1111
Source feed: FDA_Inspections

> FDA Inspection 750738 for Asahi Roentgen Ind. Co., Ltd on September 15, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 750738
- Company Name: Asahi Roentgen Ind. Co., Ltd
- Inspection Date: 2011-09-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 750738 - 2011-09-15](https://www.keypedia.com/records/fda_inspections/asahi-roentgen-ind-co-ltd/aee3fbe8-834c-4738-9554-9b2b07356938)
- [FDA Inspection 750738 - 2011-09-15](https://www.keypedia.com/records/fda_inspections/asahi-roentgen-ind-co-ltd/7aa81be8-91ea-4e44-a4d0-0227ba55653f)

Company: https://www.keypedia.com/companies/asahi-roentgen-ind-co-ltd/326a9dcc-a832-4744-bee5-716027730663

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