483
Trifluent Pharma, LLCTrifluent Pharma, LLC – FDA 483, Jun 11, 2026
Record Details
Trifluent Pharma LLC, a repacker in San Antonio, TX, was cited for two significant issues during an FDA inspection. The firm lacked adequate written procedures for controlling and reconciling labeling during repackaging operations. Additionally, the inspection revealed a failure to implement a continuing GMP training program for employees involved in packaging, labeling, and quality-related activities.
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ID · 75798d1e-d637-4221-9e3b-83d49a24fa0e
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