# FDA Inspection 982478 - Arkray Factory USA, Inc. - August 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/arkray-factory-usa-inc/cc1830c3-d932-4ec0-9b36-7831186707d6
Source feed: FDA_Inspections

> FDA Inspection 982478 for Arkray Factory USA, Inc. on August 16, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 982478
- Company Name: Arkray Factory USA, Inc.
- Inspection Date: 2016-08-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 802435 - 2012-10-16](https://www.keypedia.com/records/fda_inspections/arkray-factory-usa-inc/37b1b719-8cf2-4391-8c03-28b4443e4924)
- [FDA Inspection 736527 - 2011-07-22](https://www.keypedia.com/records/fda_inspections/arkray-factory-usa-inc/f9fdae6f-5525-4d85-9070-8b67209c91ca)

Company: https://www.keypedia.com/companies/arkray-factory-usa-inc/93ee4304-e289-4360-b1cb-8c41e3dc446e

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