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FDA Inspection
•Novartis Pharmaceuticals Corporation•February 25, 2011

Novartis Pharmaceuticals Corporation – FDA Inspection, Feb 25, 2011

Record Details

This FDA Inspection record concerns Novartis Pharmaceuticals Corporation, with an inspection on February 25, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Novartis Pharmaceuticals Corporation
Inspection Date
February 25, 2011
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 90cba958-0b54-4e35-aef1-8449422becfd

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
715718
FDA center
Human Drugs
Project area
Bioresearch Monitoring

FDA Citations

2
  1. 21 CFR 312.56(b)Investigator non-compliance
  2. 21 CFR 312.50General responsibilities of sponsors

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Novartis Pharmaceuticals Corporation

30
DateClassificationOfficeProject area
June 24, 2026Not classifiedNew Jersey District Office
June 25, 2025NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
March 3, 2025Not classifiedNew Jersey District Office
November 19, 2024Not classifiedNew Jersey District Office
August 29, 2024NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
View all 30 other inspections on the company page
Other documents for Novartis Pharmaceuticals Corporation
  • FDA Inspection 1328008 - 2026-06-24
  • FDA Inspection 1276202 - 2025-06-25
  • FDA Inspection 1263198 - 2025-03-03
  • FDA Inspection 1257911 - 2024-11-19
  • FDA Inspection 1248433 - 2024-08-29

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