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Home » Sun Pharma Lands 483 As GMP Deficiencies Continue to Plague Facility
Sun Pharma Lands 483 As GMP Deficiencies Continue to Plague Facility
Nearly a year after Sun Pharma began implementing a remediation plan to resolve GMP deficiencies at its Halol, India facility, the FDA continues to fault the company for failing to establish and maintain quality controls in a nine-observation Form 483.
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