# FDA Inspection 1114226 - Vitrolife, Inc. - December 09, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/daa5a40b-35cc-4483-bad9-c56232ee048f
Source feed: FDA_Inspections

> FDA Inspection 1114226 for Vitrolife, Inc. on December 09, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1114226
- Company Name: Vitrolife, Inc.
- Inspection Date: 2019-12-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1114226 - 2019-12-09](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/708d8a5d-61bb-41f8-abe7-6c01f1108712)
- [FDA Inspection 1079738 - 2019-02-13](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/e77ee038-3f14-4d38-abc4-eaf4b491dda5)
- [FDA Inspection 1079738 - 2019-02-13](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/8909046e-773c-4673-b618-069d9c423ffd)
- [FDA Inspection 884477 - 2014-06-05](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/a0f7ae1f-e0dd-4a22-8299-1c3d88b7f829)
- [FDA Inspection 884477 - 2014-06-05](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/d2ff37d4-a003-458d-ae34-105cf6d084cf)

Company: https://www.globalkeysolutions.net/companies/vitrolife-inc/c68ca9d8-493a-425f-a9fc-5521dbbc05dc

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