# FDA Inspection 816710 - RTX A/S - January 29, 2013

Source: https://www.keypedia.com/records/fda_inspections/rtx-as/55dfaa20-ebc5-40e1-85bb-dc8dde229d0f
Source feed: FDA_Inspections

> FDA Inspection 816710 for RTX A/S on January 29, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 816710
- Company Name: RTX A/S
- Inspection Date: 2013-01-29
- 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 816710 - 2013-01-29](https://www.keypedia.com/records/fda_inspections/rtx-as/422d2332-d05a-4e3e-b819-5c8c6e98c520)

Company: https://www.keypedia.com/companies/rtx-as/7e385035-c025-4f00-8f67-a4bd008c4831

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