# FDA Inspection 879333 - Vitrolife Inc. - May 08, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/d4810c92-8401-462b-9c6f-0261f6dc96b0
Source feed: FDA_Inspections

> FDA Inspection 879333 for Vitrolife Inc. on May 08, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 879333
- Company Name: Vitrolife Inc.
- Inspection Date: 2014-05-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/vitrolife-inc/386a7084-7769-4be3-9a8e-9495a5ca7615

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