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FDA Inspection
•SUN PHARMACEUTICAL INDUSTRIES INC•March 20, 2017

SUN PHARMACEUTICAL INDUSTRIES INC – FDA Inspection, Mar 20, 2017

Record Details

This FDA Inspection record concerns SUN PHARMACEUTICAL INDUSTRIES INC, with an inspection on March 20, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
SUN PHARMACEUTICAL INDUSTRIES INC
Inspection Date
March 20, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Parul M. Patel (Company Rep)
  • Yvesna C. Blaise (Issuing Officer)
View Company Profile

ID · c5afb702-c14c-4571-9e4e-2d464a194e41

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1005521
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.188(b)(11)Identification of Persons Performing Significant Steps

Full citation text and observation details available on the Dashboard.

Other FDA inspections of SUN PHARMACEUTICAL INDUSTRIES INC

13
DateClassificationOfficeProject area
July 24, 2026Not classifiedNew Jersey District OfficeBioresearch Monitoring
December 12, 2024NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
August 10, 2022NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
March 8, 2019NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
September 18, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 13 other inspections on the company page
Other documents for SUN PHARMACEUTICAL INDUSTRIES INC
  • FDA Inspection 1328400 - 2026-07-24
  • FDA Inspection 1230974 - 2024-12-12
  • FDA Inspection 1179668 - 2022-08-10
  • FDA Inspection 1083409 - 2019-03-08
  • FDA Inspection 1068971 - 2018-09-18

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