# FDA Inspection 590121 - Amd Ritmed - May 08, 2009

Source: https://www.keypedia.com/records/fda_inspections/amd-ritmed/5afc9ef2-d6e1-49f4-b7e4-55b445d47434
Source feed: FDA_Inspections

> FDA Inspection 590121 for Amd Ritmed on May 08, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 590121
- Company Name: Amd Ritmed
- Inspection Date: 2009-05-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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