# FDA Inspection 1086833 - SurGenTec, LLC - April 18, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/surgentec-llc/26c2eee2-128d-4ed0-be4d-9578c571b8f3
Source feed: FDA_Inspections

> FDA Inspection 1086833 for SurGenTec, LLC on April 18, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1086833
- Company Name: SurGenTec, LLC
- Inspection Date: 2019-04-18
- Classification: Voluntary Action Indicated (VAI)
- 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/surgentec-llc/75555d07-66bb-43c4-9fc8-e3dc25aac38a

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