# FDA Inspection 636405 - Hemosphere, Inc. - December 04, 2009

Source: https://www.keypedia.com/records/fda_inspections/hemosphere-inc/56d3db15-76c2-45ee-9835-89ba1c3cc08c
Source feed: FDA_Inspections

> FDA Inspection 636405 for Hemosphere, Inc. on December 04, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 636405
- Company Name: Hemosphere, Inc.
- Inspection Date: 2009-12-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 791935 - 2012-07-20](https://www.keypedia.com/records/fda_inspections/hemosphere-inc/683394b2-8830-4206-9909-98519c4b5c31)

Company: https://www.keypedia.com/companies/hemosphere-inc/3dcd4490-a581-4741-bd5d-37556adf51f9

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