Sun Pharmaceutical Industries announced that america FDA performed a Good Manufacturing Practices (GMP) inspection of Sun Pharmaceutical Industries Limited’s Halol facility (Gujarat, India) from April 26 to May 9, 2022. At the conclusion of the inspection, america FDA issued a Form-483, with 10 observations. The Company is getting ready the reaction to the observations, that allows you to be submitted to the US FDA inside 15 commercial enterprise days. The Company is dedicated to addressing
these observations right away. The Company stays committed to working closely with the US FDA and maintains to beautify its GMP compliance on an ongoing basis.
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