FDA EIR - Brenntag Southwest, Inc - August 07, 2015

An FDA inspection was conducted at Brenntag Southwest, Inc. in Oklahoma City on August 7, 2015. The purpose of the inspection was to assess the firm's compliance with 21 CFR Part 110, which outlines Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food. Brenntag Southwest operates as an ambient warehouse distributor, handling both industrial chemicals and limited food ingredients, specifically citric acid and granulated sugar, which are received from out-of-state and distributed to food manufacturers. The inspection revealed no significant violations or objectionable conditions. Consequently, a Form FDA 483, typically issued for observed deficiencies, was not issued to the firm at the conclusion of the inspection. While employees receive general worker safety training, it was noted they do not currently receive specific Good Manufacturing Practice (GMP) training related to food storage and distribution. However, this observation did not lead to a formal regulatory action. The facility was found to be clean, and pest control measures were in place. The firm also maintains a written recall plan and conducts mock recalls. In conclusion, the inspection resulted in a "No Action Indicated" classification, signifying that the firm was operating in compliance with the assessed food safety regulations during the inspection period. No specific corrective actions were required by the FDA.