# FDA Inspection 683918 - Zoncoarm - September 28, 2010

Source: https://www.keypedia.com/records/fda_inspections/zoncoarm/c7e26089-7be2-477b-a66d-38e0f530bb0e
Source feed: FDA_Inspections

> FDA Inspection 683918 for Zoncoarm on September 28, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 683918
- Company Name: Zoncoarm
- Inspection Date: 2010-09-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/zoncoarm/40c2f92e-f262-4e44-9c11-9dd44174b8fa

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