The FDA this week released a warning letter it sent to Becton Dickinson (NYSE: BDX) last month over issues it found at the company’s Franklin, Wisc.-based facilities, which produces pre-filled Heparin and 0.9% sodium chloride lock flush syringes.
The warning letter came from an inspection of the facilities which took place between May 16, 2018 and August 1, 2018, and includes a response from BD that the federal watchdog received on August 21 this year.
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