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FDA Inspection
•XF Enterprises Inc dba Xtra Factors•January 29, 2016

XF Enterprises Inc dba Xtra Factors – FDA Inspection, Jan 29, 2016

Record Details

This FDA Inspection record concerns XF Enterprises Inc dba Xtra Factors, with an inspection on January 29, 2016, issued by the Center for Veterinary Medicine, covering veterinary.

Company
XF Enterprises Inc dba Xtra Factors
Inspection Date
January 29, 2016
Product Type
Veterinary
Office
Center for Veterinary Medicine
View Company Profile

ID · 82a8e73a-3887-4780-a8f2-f55b7fdc989c

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
959554
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices

FDA Citations

6
  1. 21 CFR 225.165Cleanout procedures
  2. 21 CFR 225.65(b)Prevention of unsafe contamination by equipment
  3. 21 CFR 225.120Vermin and pest infestation
  4. 21 CFR 225.30(b)(1)Equipment capability to produce a medicated feed
  5. 21 CFR 225.202Adequacy of Records
  6. 21 CFR 225.102(b)(4)Production record discrepancy investigation and corrective action

Full citation text and observation details available on the Dashboard.

Other FDA inspections of XF Enterprises Inc dba Xtra Factors

5
DateClassificationOfficeProject area
January 17, 2024VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
February 12, 2018Not classifiedKansas City District Office
November 3, 2016VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
March 19, 2012NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
June 24, 2011VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for XF Enterprises Inc dba Xtra Factors
  • FDA Inspection 1227130 - 2024-01-17
  • FDA Inspection 1045678 - 2018-02-12
  • FDA Inspection 992696 - 2016-11-03
  • FDA Inspection 772858 - 2012-03-19
  • FDA Inspection 731051 - 2011-06-24

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Contact
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Scranton Office:
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