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FDA Inspection
•NorMed•May 29, 2025

NorMed – FDA Inspection, May 29, 2025

Record Details

This FDA Inspection record concerns NorMed, with an inspection on May 29, 2025, issued by the Seattle District Office, covering human drugs.

Company
NorMed
Inspection Date
May 29, 2025
Product Type
Human Drugs
Office
Seattle District Office
People
  • Aranjeet Singh (Company Rep)
  • Christopher R. Czajka (FDA Associated Person)
  • Thuy Tram L. Nguyen (Issuing Officer)
View Company Profile

ID · 8a23a124-f93d-4eeb-b277-14a69306095d

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1271198
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

2
  1. 21 CFR 211.142(b)Storage under appropriate conditions
  2. 21 CFR 211.84(d)(2)Reports of Analysis (Components)

Full citation text and observation details available on the Dashboard.

Other FDA inspections of NorMed

3
DateClassificationOfficeProject area
January 16, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 12, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 22, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for NorMed
  • FDA Inspection 1037662 - 2018-01-16
  • FDA Inspection 809893 - 2012-12-12
  • FDA Inspection 734357 - 2011-06-22

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