# FDA Inspection 954609 - Opgen, Inc. - November 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/opgen-inc/63a1522e-54f3-4065-8f32-99230ac3b6fb
Source feed: FDA_Inspections

> FDA Inspection 954609 for Opgen, Inc. on November 19, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 954609
- Company Name: Opgen, Inc.
- Inspection Date: 2015-11-19
- 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/opgen-inc/8129b6f8-abcd-4b9d-943e-e91ff50ee2b9

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