# FDA Inspection 1020325 - Enercon - August 03, 2017

Source: https://www.keypedia.com/records/fda_inspections/enercon/2aef89a2-930b-43f0-9aa4-ef682fe12850
Source feed: FDA_Inspections

> FDA Inspection 1020325 for Enercon on August 03, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020325
- Company Name: Enercon
- Inspection Date: 2017-08-03
- 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/enercon/24c06cf5-a7dc-42b3-b590-780716cd8047

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