# Vitrolife, Inc. - Inspection Records

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

> Inspection records and compliance data for Vitrolife, Inc. in Englewood, Colorado. Access full analysis and detailed observations.

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## Details

- Name: Vitrolife, Inc.
- FEI Number: 3003274090
- City: Englewood
- State: Colorado
- Country Name: United States
- Address Line 1: 3601 S Inca St
- Zip Code: 80110

## Related Documents

- [FDA Inspection 1114226 - Vitrolife, Inc. - 2019-12-09](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/708d8a5d-61bb-41f8-abe7-6c01f1108712) — classification: No Action Indicated (NAI), source: FDA, date: December 9, 2019
- [FDA Inspection 1114226 - Vitrolife, Inc. - 2019-12-09](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/daa5a40b-35cc-4483-bad9-c56232ee048f) — classification: No Action Indicated (NAI), source: FDA, date: December 9, 2019
- [483 - Vitrolife, Inc. - 2019-02-13](https://www.globalkeysolutions.net/records/483/vitrolife-inc/486d7fba-1308-4099-81fc-0e6f9788bdaa) — source: FDA, date: February 13, 2019
- [FDA Inspection 1079738 - Vitrolife, Inc. - 2019-02-13](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/e77ee038-3f14-4d38-abc4-eaf4b491dda5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 13, 2019
- [FDA Inspection 1079738 - Vitrolife, Inc. - 2019-02-13](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/8909046e-773c-4673-b618-069d9c423ffd) — classification: No Action Indicated (NAI), source: FDA, date: February 13, 2019
- [FDA Inspection 884477 - Vitrolife, Inc. - 2014-06-05](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/a0f7ae1f-e0dd-4a22-8299-1c3d88b7f829) — classification: No Action Indicated (NAI), source: FDA, date: June 5, 2014
- [FDA Inspection 884477 - Vitrolife, Inc. - 2014-06-05](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/d2ff37d4-a003-458d-ae34-105cf6d084cf) — classification: No Action Indicated (NAI), source: FDA, date: June 5, 2014
- [FDA Inspection 657587 - Vitrolife, Inc. - 2010-04-16](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/25566db1-2a97-48a2-b122-3885307ace81) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 16, 2010
- [FDA Inspection 657587 - Vitrolife, Inc. - 2010-04-16](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/2348926c-80b7-4081-b034-55b700fa4951) — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2010

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