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FDA Inspection
•Veranova LP•March 8, 2019

Veranova LP – FDA Inspection, Mar 8, 2019

Record Details

This FDA Inspection record concerns Veranova LP, with an inspection on March 8, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Veranova LP
Inspection Date
March 8, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Nancy M. Espinal (FDA Associated Person)
View Company Profile

ID · 4d873c8b-d46e-42e0-9e06-07d5482b6b4f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1081817
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Veranova LP

7
DateClassificationOfficeProject area
January 23, 2026Not classifiedNew Jersey District Office
February 15, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 31, 2018VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
May 5, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 31, 2013NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 7 other inspections on the company page
Other documents for Veranova LP
  • FDA Inspection 1300160 - 2026-01-23
  • FDA Inspection 1197654 - 2023-02-15
  • FDA Inspection 1040846 - 2018-01-31
  • FDA Inspection 968447 - 2016-05-05
  • FDA Inspection 853338 - 2013-10-31

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