FDA Inspection
Amoli Organics (A Division of Umedica Laboratories Pvt Ltd)Amoli Organics (A Division of Umedica Laboratories Pvt Ltd) – FDA Inspection, Sep 30, 2010
Record Details
This FDA Inspection record concerns Amoli Organics (A Division of Umedica Laboratories Pvt Ltd), with an inspection on September 30, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- September 30, 2010
- Product Type
- Drugs
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ID · afc9b404-2eb0-4a57-8876-3e6de23367ab
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 684841
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Amoli Organics (A Division of Umedica Laboratories Pvt Ltd)
5| Date | Classification | Office | Project area |
|---|---|---|---|
| March 4, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 20, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 31, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 12, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 24, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Amoli Organics (A Division of Umedica Laboratories Pvt Ltd)
- FDA Inspection 1231931 - 2024-03-04
- FDA Inspection 1065141 - 2018-07-20
- FDA Inspection 1018720 - 2017-03-31
- FDA Inspection 957768 - 2016-02-12
- FDA Inspection 878346 - 2014-04-24
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