# FDA Inspection 1120306 - ONCORE - SAN MARCOS dba NEOTECH - March 06, 2020

Source: https://www.globalkeysolutions.net/records/fda_inspections/oncore-san-marcos-dba-neotech/8a5680ef-53a3-48f6-ac1f-df76bbbbb3ba
Source feed: FDA_Inspections

> FDA Inspection 1120306 for ONCORE - SAN MARCOS dba NEOTECH on March 06, 2020. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1120306
- Company Name: ONCORE - SAN MARCOS dba NEOTECH
- Inspection Date: 2020-03-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/oncore-san-marcos-dba-neotech/d8b66587-e912-4677-a5fa-51846eacca5c

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