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FDA Inspection
•Perrigo New York, Inc.•January 22, 2019

Perrigo New York, Inc. – FDA Inspection, Jan 22, 2019

Record Details

This FDA Inspection record concerns Perrigo New York, Inc., with an inspection on January 22, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Perrigo New York, Inc.
Inspection Date
January 22, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Mindy M. Chou (FDA Associated Person)
View Company Profile

ID · a4d8e3f1-8d52-4fd2-beee-8e2a63d5b049

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1076782
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.192Investigations of discrepancies, failures
  2. 21 CFR 211.67(b)Written procedures fail to include

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Perrigo New York, Inc.

9
DateClassificationOfficeProject area
May 8, 2026VAINew York District OfficeDrug Quality Assurance
September 17, 2024Not classifiedNew York District Office
October 24, 2022VAICenter for Devices and Radiological HealthCompliance: Devices
March 8, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 22, 2015NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 9 other inspections on the company page
Other documents for Perrigo New York, Inc.
  • FDA Inspection 1316190 - 2026-05-08
  • FDA Inspection 1230391 - 2024-09-17
  • FDA Inspection 1182302 - 2022-10-24
  • FDA Inspection 1003848 - 2017-03-08
  • FDA Inspection 925558 - 2015-04-22

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Contact
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Brooklyn, NY 11201
Scranton Office:
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Scranton, PA, 18503
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