# FDA Inspection 620149 - Cardiostream, LLC - June 29, 2009

Source: https://www.keypedia.com/records/fda_inspections/cardiostream-llc/7336b189-bdbe-4c18-80ef-4a70066cf2f7
Source feed: FDA_Inspections

> FDA Inspection 620149 for Cardiostream, LLC on June 29, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 620149
- Company Name: Cardiostream, LLC
- Inspection Date: 2009-06-29
- 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 910035 - 2015-01-14](https://www.keypedia.com/records/fda_inspections/cardiostream-llc/0be9de8c-3a35-49aa-a4bd-d9b8875e7461)
- [FDA Inspection 620149 - 2009-06-29](https://www.keypedia.com/records/fda_inspections/cardiostream-llc/b846a9fc-1fd3-42cc-b01a-ae46e4af408d)

Company: https://www.keypedia.com/companies/cardiostream-llc/e5db3e89-2a42-4005-9df9-46f75dfa87a3

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