FDA Warning Wire: Zimmer Biomet Zapped Again
Here’s this week’s roundup of FDA enforcement actions.
Zimmer Zinged Again
The FDA issued yet another so-called Form 483 report, made public Tuesday, laying out its findings from an inspection of Zimmer Biomet’s Warsaw, Indiana, plant in October.
At the top of its list of 12 objectionable procedures inspectors observed at the plant...
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