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FDA Inspection
•Elite Laboratories Inc.•April 24, 2017

Elite Laboratories Inc. – FDA Inspection, Apr 24, 2017

Record Details

This FDA Inspection record concerns Elite Laboratories Inc., with an inspection on April 24, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Elite Laboratories Inc.
Inspection Date
April 24, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Niketa Patel (FDA Associated Person)
  • Tamil Arasu (FDA Associated Person)
View Company Profile

ID · cd263b5f-0f81-4d6f-b48c-1064e947d029

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1014880
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Elite Laboratories Inc.

10
DateClassificationOfficeProject area
August 1, 2025Not classifiedNew Jersey District Office
March 13, 2020VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
January 21, 2020NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 28, 2018Not classifiedNew Jersey District Office
February 2, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 10 other inspections on the company page
Other documents for Elite Laboratories Inc.
  • FDA Inspection 1269549 - 2025-08-01
  • FDA Inspection 1120647 - 2020-03-13
  • FDA Inspection 1119158 - 2020-01-21
  • FDA Inspection 1069135 - 2018-09-28
  • FDA Inspection 1042332 - 2018-02-02

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