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Previously, TBI and post-traumatic stress disorder couldn’t be effectively identified because they share similar symptoms, study co-author says. Read More
The FDA handed Siemens Medical Solutions USA a Form 483 for failing to report device malfunctions that could present health risks on at least four occasions between 2011 and 2014. Read More
Dental products manufacturer Insert Depot received a Form 483 for not properly reviewing complaints, lacking device history records, failing to establish procedures for design control and failing to ensure equipment is routinely calibrated, inspected and maintained. Read More