# FDA Inspection 1000599 - Eurofins MWG Operon, LLC - December 15, 2016

Source: https://www.keypedia.com/records/fda_inspections/eurofins-mwg-operon-llc/778f0b26-4c21-4fe6-83ed-100b1284319b
Source feed: FDA_Inspections

> FDA Inspection 1000599 for Eurofins MWG Operon, LLC on December 15, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000599
- Company Name: Eurofins MWG Operon, LLC
- Inspection Date: 2016-12-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/eurofins-mwg-operon-llc/a6a5ccf5-ed42-47a9-bce9-33ee1f314327

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