FDA: 1 company in cities within Faulkner County received 8 citations in 2025

Jim Traficant, Chief of Staff of FDA
Jim Traficant, Chief of Staff of FDA
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There was one company in a city associated with Faulkner County that received FDA citations as a result of one inspection conducted in the county in 2025, according to the U.S. Food and Drug Administration (FDA).

This is unchanged from the number of companies cited in the previous year.

The citations in the county include:

  • Employees engaged in the manufacture and processing of a drug product lack the training and experience required to perform their assigned functions.
  • Your firm failed to establish written procedures for production and process controls designed to assure that the drug products have the identity, strength, purity, and quality that they are purported or represented to possess.
  • Control procedures are not established which validate the performance of those manufacturing processes that may be responsible for causing variability in the characteristics of in-process material and the drug product.

The company cited was involved in the Drugs sector.

The company cited had to take regulatory and/or administrative actions.

The FDA routinely inspects facilities across the nation to determine if the workplace and their products are compliant with FDA-regulated laws and regulations implemented to improve overall public health. Inspection results are then disclosed publicly.

According to its website, the FDA is a government agency that is primarily responsible for monitoring the production and distribution of human and animal drugs, biological products, medical supplies and tobacco products for safety and quality.

Companies Located within Faulkner County Cities and the Citations They Received in 2025
Company Name Area of Business Inspection Date Issue Cited
Turbare Manufacturing Drugs 01/24/2025 Training , Education , Experience overall
Turbare Manufacturing Drugs 01/24/2025 Absence of Written Procedures
Turbare Manufacturing Drugs 01/24/2025 Control procedures to monitor and validate performance
Turbare Manufacturing Drugs 01/24/2025 Procedures for sterile drug products
Turbare Manufacturing Drugs 01/24/2025 Validation lacking for sterile drug products
Turbare Manufacturing Drugs 01/24/2025 Acceptance criteria for sampling & testing
Turbare Manufacturing Drugs 01/24/2025 Investigations of discrepancies, failures
Turbare Manufacturing Drugs 01/24/2025 Second person sign off

Information in this article was obtained from the U.S. Food and Drug Administration. The source data can be found here.



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