FDA 483 - Frito-Lay Inc - March 22, 2021

Frito-Lay Inc. received a Form 483 due to significant deficiencies in its allergen control procedures, particularly concerning packaging film management. The firm failed to implement adequate corrective actions following a recall event, and its monitoring and labeling controls were found to be insufficient. These issues indicate a high severity regarding potential allergen cross-contamination and mislabeling.