FDA establishment 3002807511, Mandideep, India. Part of Lupin's FDA records. Every inspection FDA has posted for the site, with its outcome and cited regulations.
FY2018 to FY2027 to date; 2 classified OAI
A hatched bar is a year that is not over, so its count covers only part of the year.
| Ended | Product and area | Citations | Classification |
|---|---|---|---|
| Nov 23, 2022 | Drugs · Drug Quality Assurance | None posted | Official Action Indicated (OAI) |
| Dec 4, 2018 | Drugs · Drug Quality Assurance | None posted | Official Action Indicated (OAI) |
| Feb 19, 2016 | Drugs · Drug Quality Assurance | None posted | Voluntary Action Indicated (VAI) |
| Sep 23, 2011 | Drugs · Drug Quality Assurance | None posted | Voluntary Action Indicated (VAI) |
| Nov 30, 2009 | Drugs · Drug Quality Assurance | None posted | Voluntary Action Indicated (VAI) |
| Nov 12, 2008 | Drugs · Drug Quality Assurance | None posted | Official Action Indicated (OAI) |
An FEI (FDA Establishment Identifier) names one physical site. Inspections, outcomes and citations come from FDA's Data Dashboard; FDA posts citations only for some inspections. Recalls come from FDA's enforcement reports (iRES), one row per recall even when it covers many lots. A contract site can make products for many companies, so the company shown is the one FDA lists as the site's firm. FDA Data Dashboard, warning letters and enforcement reports
Mandideep, India. Part of