# FDA Inspection 858240 - Pathfinder Cell Therapy, Inc. - December 04, 2013

Source: https://www.keypedia.com/records/fda_inspections/pathfinder-cell-therapy-inc/675d92d4-83b9-4ac6-bc73-c9114524f580
Source feed: FDA_Inspections

> FDA Inspection 858240 for Pathfinder Cell Therapy, Inc. on December 04, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 858240
- Company Name: Pathfinder Cell Therapy, Inc.
- Inspection Date: 2013-12-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 652314 - 2010-03-18](https://www.keypedia.com/records/fda_inspections/pathfinder-cell-therapy-inc/3ee91188-261e-47e5-81ac-4e2747b58cee)
- [FDA Inspection 652314 - 2010-03-18](https://www.keypedia.com/records/fda_inspections/pathfinder-cell-therapy-inc/96c3de33-d37d-472f-ad58-fb82183edc67)

Company: https://www.keypedia.com/companies/pathfinder-cell-therapy-inc/13b48bba-5413-43fc-b174-d1b29a7aba47

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