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FDA Inspection
•Northland Nuclear Medicine, LLC•June 7, 2019

Northland Nuclear Medicine, LLC – FDA Inspection, Jun 7, 2019

Record Details

This FDA Inspection record concerns Northland Nuclear Medicine, LLC, with an inspection on June 7, 2019, issued by the Minneapolis District Office, covering human drugs.

Company
Northland Nuclear Medicine, LLC
Inspection Date
June 7, 2019
Product Type
Human Drugs
Office
Minneapolis District Office
People
  • Anthony J. Ladner (FDA Associated Person)
  • Scott A. Golladay
View Company Profile

ID · 1d9a3582-f77c-4de9-b9c2-80c2cd2bbb27

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1092563
FDA center
Human Drugs
Project area
Generic Drug Evaluation
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 212.30(b)Equipment procedures
  2. 21 CFR 212.50Adequate controls (general)
  3. 21 CFR 212.50(b)Master Production and Control Records

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Northland Nuclear Medicine, LLC

1
DateClassificationOfficeProject area
July 13, 2023OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Northland Nuclear Medicine, LLC
  • FDA Inspection 1210014 - 2023-07-13

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