# Eurotrol B. V. – FDA Inspection, May 6, 2016

Source: https://www.keypedia.com/records/fda_inspections/eurotrol-b-v/1dfd1cf2-0cc9-4bbc-80b7-db71db63658e
Source feed: FDA_Inspections

> FDA inspection 972348 of Eurotrol B. V., May 06, 2016. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 972348
- Company Name: Eurotrol B. V.
- Inspection Date: 2016-05-06
- 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: 7

## Related Documents

- [FDA Inspection 883233 - 2014-05-22](https://www.keypedia.com/records/fda_inspections/eurotrol-b-v/c7943876-5ffc-4703-addb-40fa5ccaf1af)

Company: https://www.keypedia.com/companies/eurotrol-b-v/56a31f09-d312-4487-8135-b1658d2d89e0

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