# Fairfax Cryobank, Inc., Austin, TX – FDA Inspections

Source: https://www.keypedia.com/companies/fairfax-cryobank-inc/d31a3e45-800d-456e-9a8f-d047b7eb2e22

> Inspection records and compliance data for Fairfax Cryobank, Inc. in Austin, Texas. 6 FDA inspections on record, last inspected September 10, 2025.

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## Details

- Name: Fairfax Cryobank, Inc.
- FEI Number: 3005033855
- Address Line 1: 1305 W 34th St Ste 210
- City: Austin
- State: Texas
- Zip Code: 78705
- Country Name: United States
- Address: 1305 W 34th St Ste 210, Austin, Texas 78705, United States
- Country: United States

## Related Documents

- FDA Inspection 1292744 - Fairfax Cryobank, Inc. - 2025-09-10 — source: FDA, date: September 10, 2025
- [FDA Inspection 1292744 - Fairfax Cryobank, Inc. - 2025-09-10](https://www.keypedia.com/records/fda_inspections/fairfax-cryobank-inc/d55441e6-5160-4ea7-af87-147f6de54713) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2025
- FDA Inspection 1151719 - Fairfax Cryobank, Inc. - 2021-09-09 — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2021
- FDA Inspection 1151719 - Fairfax Cryobank, Inc. - 2021-09-09 — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2021
- FDA Inspection 1151719 - Fairfax Cryobank, Inc. - 2021-09-09 — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2021
- FDA Inspection 1050840 - Fairfax Cryobank, Inc. - 2018-04-05 — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2018
- FDA Inspection 1050840 - Fairfax Cryobank, Inc. - 2018-04-05 — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2018
- FDA Inspection 872774 - Fairfax Cryobank, Inc. - 2014-04-02 — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2014
- FDA Inspection 771265 - Fairfax Cryobank, Inc. - 2012-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2012
- FDA Inspection 553060 - Fairfax Cryobank, Inc. - 2008-11-20 — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2008

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