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FDA Inspection
•Hetero Labs Ltd. Unit VI•November 15, 2016

Hetero Labs Ltd. Unit VI – FDA Inspection, Nov 15, 2016

Record Details

This FDA Inspection record concerns Hetero Labs Ltd. Unit VI, with an inspection on November 15, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Hetero Labs Ltd. Unit VI
Inspection Date
November 15, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Michael E. Maselli (Company Rep)
  • Yasamin Ameri (FDA Associated Person)
View Company Profile

ID · 4427e13b-4ca3-4730-b696-ef5df9aee016

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
999209
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Hetero Labs Ltd. Unit VI

2
DateClassificationOfficeProject area
September 21, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 23, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Hetero Labs Ltd. Unit VI
  • FDA Inspection 1218220 - 2023-09-21
  • FDA Inspection 833134 - 2013-05-23

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