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FDA Inspection
•Veranova LP•January 23, 2026

Veranova LP – FDA Inspection, Jan 23, 2026

Record Details

This FDA Inspection record concerns Veranova LP, with an inspection on January 23, 2026, issued by the New Jersey District Office, covering human drugs.

Company
Veranova LP
Inspection Date
January 23, 2026
Product Type
Human Drugs
Office
New Jersey District Office
People
  • Catherine O. Lamptey (Company Rep)
  • David A. Oluwo (FDA Associated Person)
  • Michael O. Idowu (Company Rep)
View Company Profile

ID · 732c92fe-b2f5-4217-837b-98894814148f

Inspection Facts

Inspection number
1300160
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Veranova LP

7
DateClassificationOfficeProject area
February 15, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 8, 2019VAICenter 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 1197654 - 2023-02-15
  • FDA Inspection 1081817 - 2019-03-08
  • FDA Inspection 1040846 - 2018-01-31
  • FDA Inspection 968447 - 2016-05-05
  • FDA Inspection 853338 - 2013-10-31

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
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