# FDA Inspection 934069 - Neomend Inc - June 18, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/neomend-inc/ff0f4abf-04f1-4473-ba8c-7eedd4d65179/
Source feed: FDA_Inspections

> FDA Inspection 934069 for Neomend Inc on June 18, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 934069
- Company Name: Neomend Inc
- Inspection Date: 2015-06-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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