FDA Warning Wire: Zimmer Rapped In Inspection, Again
Law360, New York (January 24, 2017, 8:35 PM EST) -- The U.S. Food and Drug Administration again found issues with one of medical device maker Zimmer Biomet’s plants, took a British drug maker to task over the presence of metal particles in a leukemia drug and criticized fishy safety protocols at an Icelandic fishery.
Here’s this week’s roundup of the agency’s enforcement actions
Zimmer Biomet Faulted For Plant Conditions, Again
The FDA issued one of its so-called Form 483 reports detailing, in nearly 60 heavily redacted pages, its findings from an inspection of Zimmer Biomet’s Warsaw, Indiana, plant from September to November.
All in all, the report laid out 14 observations...
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