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FDA Inspection
•Nexus Pharmaceuticals, LLC•November 5, 2014

Nexus Pharmaceuticals, LLC – FDA Inspection, Nov 5, 2014

Record Details

This FDA Inspection record concerns Nexus Pharmaceuticals, LLC, with an inspection on November 5, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Nexus Pharmaceuticals, LLC
Inspection Date
November 5, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 32cc3842-5652-47d9-ae6e-69f963728a59

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
903661
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

2
  1. 21 CFR 211.198(a)Complaint Handling Procedure
  2. 21 CFR 211.22(a)Contract drug products--lack of responsibility

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Nexus Pharmaceuticals, LLC

6
DateClassificationOfficeProject area
June 4, 2026VAIChicago District OfficeDrug Quality Assurance
November 7, 2023NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
May 25, 2022NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 29, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 28, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Nexus Pharmaceuticals, LLC
  • FDA Inspection 1301896 - 2026-06-04
  • FDA Inspection 1224257 - 2023-11-07
  • FDA Inspection 1171206 - 2022-05-25
  • FDA Inspection 976279 - 2016-06-29
  • FDA Inspection 871664 - 2014-03-28

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