# FDA Inspection 1092633 - Silex Medical, LLC - June 11, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/silex-medical-llc/73531db1-abc2-42d4-b534-bbc8776a36f2
Source feed: FDA_Inspections

> FDA Inspection 1092633 for Silex Medical, LLC on June 11, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1092633
- Company Name: Silex Medical, LLC
- Inspection Date: 2019-06-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/silex-medical-llc/218e6dd8-5da5-44d6-a66d-2b9700bb600f

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