# FDA Inspection 583667 - Prorhythm, Inc. - May 06, 2009

Source: https://www.keypedia.com/records/fda_inspections/prorhythm-inc/1a0c249a-05d9-42d5-9e8b-e14de39448af
Source feed: FDA_Inspections

> FDA Inspection 583667 for Prorhythm, Inc. on May 06, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 583667
- Company Name: Prorhythm, Inc.
- Inspection Date: 2009-05-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 583667 - 2009-05-06](https://www.keypedia.com/records/fda_inspections/prorhythm-inc/8a2f7d88-ec5a-4f92-a9c5-065519aec862)

Company: https://www.keypedia.com/companies/prorhythm-inc/d57d625a-5f30-4a4f-992f-30ae94a83681

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