# FDA Inspection 708783 - Binder Biomedical Inc - February 04, 2011

Source: https://www.keypedia.com/records/fda_inspections/binder-biomedical-inc/e14cd38f-56fc-4569-8eea-edfb65cafce3
Source feed: FDA_Inspections

> FDA Inspection 708783 for Binder Biomedical Inc on February 04, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 708783
- Company Name: Binder Biomedical Inc
- Inspection Date: 2011-02-04
- 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 708783 - 2011-02-04](https://www.keypedia.com/records/fda_inspections/binder-biomedical-inc/52437f05-662d-44f6-bba1-330123ed4bf0)
- [FDA Inspection 665013 - 2010-06-04](https://www.keypedia.com/records/fda_inspections/binder-biomedical-inc/2a7e6964-e7c0-4f1c-9c9f-e367b2fe580e)

Company: https://www.keypedia.com/companies/binder-biomedical-inc/eca8e434-5ada-40ac-a3fd-b95fefa3ca1d

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