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Home » Impax Not Rejecting Failed Drugs, Newly Released Form 483 Highlights
Impax Not Rejecting Failed Drugs, Newly Released Form 483 Highlights
June 5, 2012
Agency inspectors found Impax Laboratories failed to reject drug products that did not meet established standards and specifications, an FDA Form 483 states, shedding light on quality issues found at the company’s troubled Hayward, Calif., facility.