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FDA Inspection
•Taro Pharmaceuticals Inc.•September 16, 2022

Taro Pharmaceuticals Inc. – FDA Inspection, Sep 16, 2022

Record Details

This FDA Inspection record concerns Taro Pharmaceuticals Inc., with an inspection on September 16, 2022, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Taro Pharmaceuticals Inc.
Inspection Date
September 16, 2022
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 5f06f6fb-7c0a-44ca-8fd5-6aad610d4a0c

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1180887
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

2
  1. 21 CFR 211.110(a)Written in-process control procedures
  2. 21 CFR 211.100(b)SOPs not followed / documented

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Taro Pharmaceuticals Inc.

7
DateClassificationOfficeProject area
March 27, 2026NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 20, 2024Not classifiedOffice of Inspections and Investigations
May 3, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 20, 2017VAIOffice of Inspections and InvestigationsGeneric Drug Evaluation
July 29, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Taro Pharmaceuticals Inc.
  • FDA Inspection 1312804 - 2026-03-27
  • FDA Inspection 1257703 - 2024-09-20
  • FDA Inspection 1088553 - 2019-05-03
  • FDA Inspection 1001628 - 2017-01-20
  • FDA Inspection 984831 - 2016-07-29

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