FDA performs inspection of Impax's Taiwan facility

30 July 2014

The US Food and Drug Administration has performed a general Good Manufacturing Practices (GMP) inspection and a Pre-Approval Inspection (PAI) at US generic drugmaker Impax Laboratories’ (Nasdaq: IPXL) manufacturing facility in Taiwan.

The inspections, carried out from July 21 to 26, came ahead of the company’s launch of Parkinson's disease drug Rytary (carbidopa/levodopa), which is awaiting FDA approval.

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