The U.S. Food and Drug Administration (U.S. FDA) has issued 11 observations to the formulation manufacturing facility of Aurobindo Pharma’s subsidiary Eugia Pharma Specialities in Hyderabad. The observations were issued on conclusion of an inspection, by the U.S. FDA, of the facility (Unit-III) from January 27 to February 6. The The observations are procedural in nature and will be responded to within the stipulated time, Aurobindo Pharma said in a filing on Friday. Published – February 06, 2026 10:10 pm IST Share this: Click to share on WhatsApp (Opens in new window) WhatsApp Click to share on Facebook (Opens in new window) Facebook Click to share on Threads (Opens in new window) Threads Click to share on X (Opens in new window) X Click to share on Telegram (Opens in new window) Telegram Click to share on LinkedIn (Opens in new window) LinkedIn Click to share on Pinterest (Opens in new window) Pinterest Click to email a link to a friend (Opens in new window) Email More Click to print (Opens in new window) Print Click to share on Reddit (Opens in new window) Reddit Click to share on Tumblr (Opens in new window) Tumblr Click to share on Pocket (Opens in new window) Pocket Click to share on Mastodon (Opens in new window) Mastodon Click to share on Nextdoor (Opens in new window) Nextdoor Click to share on Bluesky (Opens in new window) Bluesky Like this:Like Loading... Post navigation RBI plans to compensate up to ₹25,000 in online fraud losses Zydus’ Desidustat gets Orphan Drug Designation from U.S. FDA for Sickle Cell disease