Drug factory · FDA FEI 3002807586
Kindeva Drug Delivery Limited
Derby Road, Loughborough, United Kingdom
Problems found, fixed voluntarily at FDA's last inspection, Mar 14, 2025.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
8 drug inspections on record since 2009: 1 with no problems, 7 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Albuterol | Makes it | Sandoz Inc. | 0781-7296 |
| Imiquimod | Makes it | Bausch Health US, LLC, Oceanside Pharmaceuticals., Teva Pharmaceuticals USA, Inc. | 99207-270, 99207-271, 99207-276 +2 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Mar 14, 2025 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| May 27, 2021 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| May 3, 2018 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Jun 30, 2017 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Aug 12, 2016 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Mar 5, 2015 | No problems found | Drug Quality Assurance | — |
| Apr 15, 2013 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Apr 17, 2009 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: analysis; api manufacture; label; manufacture; pack; relabel; repack.