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Capital Market on MSNDr Reddys Lab receives EIR from USFDA for Middleburgh API facilityIn a regulatory filing, the company stated that the EIR was issued following a good manufacturing practice (GMP) inspection conducted by the USFDA. The inspection outcome has been classified as ...
The Food and Drug Administration announced the recall of tens of thousands of cases of deodorant. The FDA said that it was ...
The Food and Drug Administration has recalled more than 67,000 cases of deodorant sold at major retailers due to manufacturing practices that violate federal regulations. Three types of Power Sticks ...
Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by ...
Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by ...
A.P. Deauville, a Pennsylvania-based health and beauty manufacturer, has recalled more than 67,000 cases of its Power Stick ...
Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by ...
Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by ...
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not ...
WASHINGTON — Tens of thousands of cases of Power Stick deodorant have been voluntarily recalled due to a manufacturing defect ...
More than 67,000 cases of Power Stick roll-on deodorant products have been recalled. They were sold at Target, Walmart, ...
Various Power Stick deodorants have been recalled due to "Current Good Manufacturing Practice deviations", according to the U ...
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