# FDA Inspection 993759 - Aurora Manufacturing LLC - October 31, 2016

Source: https://www.keypedia.com/records/fda_inspections/aurora-manufacturing-llc/b3314c20-95d8-4d07-ba6c-e6aad1a66a29
Source feed: FDA_Inspections

> FDA Inspection 993759 for Aurora Manufacturing LLC on October 31, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993759
- Company Name: Aurora Manufacturing LLC
- Inspection Date: 2016-10-31
- 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.keypedia.com/companies/aurora-manufacturing-llc/b1364858-ecc0-4349-a668-aa897ed6b0f6

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