# FDA Inspection 649535 - Resenex Corporation - March 02, 2010

Source: https://www.keypedia.com/records/fda_inspections/resenex-corporation/2339fad0-63ff-4a6b-8270-d22e14f8779c
Source feed: FDA_Inspections

> FDA Inspection 649535 for Resenex Corporation on March 02, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 649535
- Company Name: Resenex Corporation
- Inspection Date: 2010-03-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 649535 - 2010-03-02](https://www.keypedia.com/records/fda_inspections/resenex-corporation/1eaea6d3-5606-417d-8ae8-7d8f1e263b4c)

Company: https://www.keypedia.com/companies/resenex-corporation/5634d016-1ee6-4763-b02d-f61e1431ae74

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