# Vitrolife Inc. - Inspection Records

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

> Inspection records and compliance data for Vitrolife Inc. in San Diego, California. Access full analysis and detailed observations.

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## Details

- Name: Vitrolife Inc.
- FEI Number: 3002757762
- City: San Diego
- State: California
- Country Name: United States
- Address Line 1: 6835 Flanders Dr Ste 500
- Zip Code: 92121

## Related Documents

- [483 - Vitrolife Inc. - 2025-01-23](https://www.globalkeysolutions.net/records/483/vitrolife-inc/5c2c60ef-506c-4850-ba06-09c277d5225d) — source: FDA, date: January 23, 2025
- [FDA Inspection 1259055 - Vitrolife Inc. - 2025-01-23](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/b041cd38-08ff-46e6-894f-086e1fb7f71a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 23, 2025
- [FDA Inspection 1259055 - Vitrolife Inc. - 2025-01-23](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/195a4df1-91ba-464a-b337-ae29cfbd243f) — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2025
- [FDA Inspection 1259055 - Vitrolife Inc. - 2025-01-23](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/c7e0698f-175d-4f00-a188-60ad0bf49431) — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2025
- [FDA Inspection 1259055 - Vitrolife Inc. - 2025-01-23](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/dc242a42-f0eb-4f73-bd1b-11223ed2fa25) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 23, 2025
- [483 - Vitrolife Inc. - 2021-08-19](https://www.globalkeysolutions.net/records/483/vitrolife-inc/d3e7f6ed-6646-4916-941b-847a96f1e225) — source: FDA, date: August 19, 2021
- [FDA Inspection 1149812 - Vitrolife Inc. - 2021-08-19](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/862384ef-1a36-4262-890d-9424d1c2a7a3) — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2021
- [FDA Inspection 1149812 - Vitrolife Inc. - 2021-08-19](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/08e3cb8d-911f-436d-91cd-abd62550c3ca) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 19, 2021
- [FDA Inspection 1066292 - Vitrolife Inc. - 2018-09-21](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/86a5b96e-14f6-4922-8259-71043ebb93a5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 21, 2018
- [FDA Inspection 1066292 - Vitrolife Inc. - 2018-09-21](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/6cd86ccd-7a3e-4da3-9ec6-04240de33dc9) — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2018
- [FDA Inspection 879333 - Vitrolife Inc. - 2014-05-08](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/654cc167-137f-4b06-a9b1-0d3ac11f980d) — classification: No Action Indicated (NAI), source: FDA, date: May 8, 2014
- [FDA Inspection 879333 - Vitrolife Inc. - 2014-05-08](https://www.globalkeysolutions.net/records/fda_inspections/vitrolife-inc/d4810c92-8401-462b-9c6f-0261f6dc96b0) — classification: No Action Indicated (NAI), source: FDA, date: May 8, 2014

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