# FDA Inspection 879434 - Vitrolife A/S - May 01, 2014

Source: https://www.keypedia.com/records/fda_inspections/vitrolife-as/e514c253-480b-4099-b083-de786058fbe4
Source feed: FDA_Inspections

> FDA Inspection 879434 for Vitrolife A/S on May 01, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 879434
- Company Name: Vitrolife A/S
- Inspection Date: 2014-05-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 879434 - 2014-05-01](https://www.keypedia.com/records/fda_inspections/vitrolife-as/c6ddd3fc-8147-4c03-ab90-542925b0858a)

Company: https://www.keypedia.com/companies/vitrolife-as/44407742-0b15-4ff4-909a-320fafdccbfd

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