# XF Enterprises Inc dba Xtra Factors, Pratt, KS – FDA Inspections

Source: https://www.keypedia.com/companies/xf-enterprises-inc-dba-xtra-factors/96d3047a-eed5-4c66-89f5-04bb78eb853f

> Inspection records and compliance data for XF Enterprises Inc dba Xtra Factors in Pratt, Kansas. 6 FDA inspections on record (1 OAI), 1 Form 483, last inspected January 17, 2024.

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## Details

- Name: XF Enterprises Inc dba Xtra Factors
- FEI Number: 1921258
- Address Line 1: 211 Pedigo Dr
- City: Pratt
- State: Kansas
- Zip Code: 67124
- Country Name: United States
- Address: 211 Pedigo Dr, Pratt, Kansas 67124, United States
- Country: United States

## Related Documents

- [FDA Inspection 1227130 - XF Enterprises Inc dba Xtra Factors - 2024-01-17](https://www.keypedia.com/records/fda_inspections/xf-enterprises-inc-dba-xtra-factors/9a91c9ca-b652-45fc-b498-fca6d96a50cc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 17, 2024
- FDA Inspection 1045678 - XF Enterprises Inc dba Xtra Factors - 2018-02-12 — source: FDA, date: February 12, 2018
- [FDA Inspection 992696 - XF Enterprises Inc dba Xtra Factors - 2016-11-03](https://www.keypedia.com/records/fda_inspections/xf-enterprises-inc-dba-xtra-factors/e1fd1e6c-f3db-4a2e-b099-ea59d55518ef) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 3, 2016
- [FDA Inspection 959554 - XF Enterprises Inc dba Xtra Factors - 2016-01-29](https://www.keypedia.com/records/fda_inspections/xf-enterprises-inc-dba-xtra-factors/82a8e73a-3887-4780-a8f2-f55b7fdc989c) — classification: Official Action Indicated (OAI), source: FDA, date: January 29, 2016
- FDA Inspection 772858 - XF Enterprises Inc dba Xtra Factors - 2012-03-19 — classification: No Action Indicated (NAI), source: FDA, date: March 19, 2012
- [FDA Inspection 731051 - XF Enterprises Inc dba Xtra Factors - 2011-06-24](https://www.keypedia.com/records/fda_inspections/xf-enterprises-inc-dba-xtra-factors/62fe0d53-6a15-4a51-b4e5-1e7800d40b71) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 24, 2011

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