# Aurora Manufacturing LLC – FDA Inspection, Oct 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 of Aurora Manufacturing LLC, October 31, 2016. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 834441 - 2013-04-19
- FDA Inspection 670670 - 2009-11-10

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gamal-a-norton/6b52c9e6-d579-4994-81ee-e734eb1f0a67)

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