FDA 483 - AstraZeneca Pharmaceuticals LP - July 22, 2022
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An FDA inspection of AstraZeneca Pharmaceuticals LP's vaccine manufacturing facility in Philadelphia, PA, revealed significant deficiencies in aseptic processing procedures, environmental monitoring, and equipment design. The firm also failed to adequately investigate unexplained discrepancies and extend risk assessments to other affected batches. These observations indicate a need for improved controls to prevent microbiological contamination and ensure product quality.
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