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Intas received 16 “observations” on their Form 483 inspection report.

America’s drug supply is increasingly reliant on companies who continually get failing grades from the Food & Drug Administration.

“We can’t risk patients' lives by giving them potentially bad drugs from unapproved manufacturers."

An import alert means the lab’s products are off limits to the U.S. until corrections are made to its manufacturing processes.

Shocking Decision Risks Patients Lives Battling Cancer WASHINGTON — Americans for Safe Drugs, a campaign led by the Coalition for a...

The recall was being initiated because of failures in environmental monitoring of the facility where the drugs are made.

New Report Shows FDA Inspected Just 6% of Drug Manufacturers By some estimates, well over half of America’s generic drug supply comes...

Americans at Risk of Taking Potentially Unsafe Drug from Facility Under FDA Import Ban WASHINGTON — Americans for Safe Drugs today...