We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
The FDA hit a Rockledge, Florida over-the-counter drugmaker with a warning letter over failures related to testing, quality unit oversight and water quality monitoring. Read More
OTC drugmaker Emilia Resources drew a Form 483 from the FDA for failing to validate manufacturing processes and establish data controls, among other lapses at its facility in De Kalb, Mississippi. Read More
Quality shortcomings including rusty equipment and data integrity lapses drew a warning letter from the FDA for GPT Pharmaceuticals’ facility in Hyderabad. Read More
The FDA issued a warning letter to LNK International for failing to fully investigate contaminated lots of antihistamines it released to the market. Read More