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13 Aug 2022 | |
This is to inform you that the US FDA conducted an inspection of Mohali manufacturing facility (Punjab, India) of Sun Pharmaceutical Industries Limited ('the Company') from August 3, 2022 to August 12, 2022. At the conclusion of the inspection, the US FDA issued a Form-483, with 6 observations. The Company is preparing the response to the observations, which will be submitted to US FDA within the stipulated timeline. | |
View all announcements for SUN PHARMACEUTICAL INDUSTRIES LTD. | Source: BSE India |