# FDA Inspection 626365 - Neomend Inc - November 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/neomend-inc/a57e27f9-4b60-4d2e-8003-e0d9f1fc413a
Source feed: FDA_Inspections

> FDA Inspection 626365 for Neomend Inc on November 09, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 626365
- Company Name: Neomend Inc
- Inspection Date: 2009-11-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1022919 - 2017-08-10](https://www.keypedia.com/records/fda_inspections/neomend-inc/011214b3-bd4d-4440-b993-ead2fe55f92a)
- [FDA Inspection 1022919 - 2017-08-10](https://www.keypedia.com/records/fda_inspections/neomend-inc/07a8cd97-e099-47b7-9b76-eb438f0dcdcb)
- [FDA Inspection 941850 - 2015-09-01](https://www.keypedia.com/records/fda_inspections/neomend-inc/21cf9860-6a9a-4a71-a9fa-54dacec200de)
- [FDA Inspection 934069 - 2015-06-18](https://www.keypedia.com/records/fda_inspections/neomend-inc/2c516611-0397-4a5b-ba63-590ba565c1f6)
- [FDA Inspection 934069 - 2015-06-18](https://www.keypedia.com/records/fda_inspections/neomend-inc/ff0f4abf-04f1-4473-ba8c-7eedd4d65179)

Company: https://www.keypedia.com/companies/neomend-inc/0b1ee2d6-de6e-4f5f-a599-929bb15dae7f

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