# Enercon – FDA Inspection, Aug 3, 2017

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

> FDA inspection 1020325 of Enercon, August 03, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- 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: 1

## Related Documents

- FDA Inspection 1204697 - 2023-04-19

## Related Officers

- Issuing Officer
- Issuing Officer

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