FDA establishment 3008243902, Hyderabad, India. Part of Aizant Drug Research Solutions's FDA records. Every inspection FDA has posted for the site, with its outcome and cited regulations.
FY2018 to FY2027 to date; 0 classified OAI
A hatched bar is a year that is not over, so its count covers only part of the year.
Inspections citing each reference
| Jul 31, 2026 | Drugs · Drug Quality Assurance | 3 cited references
| Voluntary Action Indicated (VAI) |
| Nov 14, 2025 | Drugs · Bioresearch Monitoring | None posted | Voluntary Action Indicated (VAI) |
| Apr 28, 2023 | Drugs · Drug Quality Assurance | None posted | No Action Indicated (NAI) |
| Jan 25, 2023 | Drugs · Bioresearch Monitoring | None posted | No Action Indicated (NAI) |
| Jan 24, 2020 | Drugs · Drug Quality Assurance | None posted | Voluntary Action Indicated (VAI) |
| May 3, 2019 | Drugs · Bioresearch Monitoring | None posted | No Action Indicated (NAI) |
| Mar 15, 2019 | Drugs · Bioresearch Monitoring | None posted | No Action Indicated (NAI) |
| Jul 13, 2018 | Drugs · Drug Quality Assurance | None posted | Voluntary Action Indicated (VAI) |
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