# FDA Inspection 819503 - Amd Ritmed - February 14, 2013

Source: https://www.keypedia.com/records/fda_inspections/amd-ritmed/ac228eae-9432-431a-8d73-61ef7fa401d0
Source feed: FDA_Inspections

> FDA Inspection 819503 for Amd Ritmed on February 14, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 819503
- Company Name: Amd Ritmed
- Inspection Date: 2013-02-14
- 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 819503 - 2013-02-14](https://www.keypedia.com/records/fda_inspections/amd-ritmed/2cf23f53-5781-4d10-b8c4-8f8c5c137195)
- [FDA Inspection 590121 - 2009-05-08](https://www.keypedia.com/records/fda_inspections/amd-ritmed/8667ef23-ff26-4af8-b315-5506ff9cd6c3)
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Company: https://www.keypedia.com/companies/amd-ritmed/00f57382-7ac3-4d29-8701-2c2dfc6db203

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