# Stellex/CF Houston, LLC, Houston, TX – FDA Inspections

Source: https://www.keypedia.com/companies/stellexcf-houston-llc/9f65121a-dcae-4442-ad13-77494785e810

> Inspection records and compliance data for Stellex/CF Houston, LLC in Houston, Texas. 8 FDA inspections on record, last inspected September 18, 2025.

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## Details

- Name: Stellex/CF Houston, LLC
- FEI Number: 1000139050
- Address Line 1: 2008 Ww Thorne Blvd
- City: Houston
- State: Texas
- Zip Code: 77073
- Country Name: United States
- Address: 2008 Ww Thorne Blvd, Houston, Texas 77073, United States
- Country: United States

## Related Documents

- FDA Inspection 1280199 - Stellex/CF Houston, LLC - 2025-09-18 — source: FDA, date: September 18, 2025
- FDA Inspection 1280199 - Stellex/CF Houston, LLC - 2025-09-18 — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2025
- FDA Inspection 1150617 - Stellex/CF Houston, LLC - 2021-08-17 — classification: No Action Indicated (NAI), source: FDA, date: August 17, 2021
- [FDA Inspection 1122094 - Stellex/CF Houston, LLC - 2020-03-11](https://www.keypedia.com/records/fda_inspections/stellexcf-houston-llc/ae618f4b-aa19-4b7c-a546-94028a4e27e8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 11, 2020
- FDA Inspection 1004989 - Stellex/CF Houston, LLC - 2017-03-06 — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2017
- FDA Inspection 800684 - Stellex/CF Houston, LLC - 2012-09-26 — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2012
- FDA Inspection 719843 - Stellex/CF Houston, LLC - 2011-04-14 — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2011
- FDA Inspection 719843 - Stellex/CF Houston, LLC - 2011-04-14 — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2011
- FDA Inspection 719843 - Stellex/CF Houston, LLC - 2011-04-14 — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2011
- FDA Inspection 661152 - Stellex/CF Houston, LLC - 2010-04-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 30, 2010

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