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FDA Inspection
•Precision Nuclear of Virginia, LLC•October 17, 2025

Precision Nuclear of Virginia, LLC – FDA Inspection, Oct 17, 2025

Record Details

This FDA Inspection record concerns Precision Nuclear of Virginia, LLC, with an inspection on October 17, 2025, issued by the Baltimore District Office, covering human drugs.

Company
Precision Nuclear of Virginia, LLC
Inspection Date
October 17, 2025
Product Type
Human Drugs
Office
Baltimore District Office
People
  • David A. Oluwo (FDA Associated Person)
  • Kara J. Wright
View Company Profile

ID · 4989c2ba-25ae-4377-bb73-16c80058f0d5

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1287392
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

2
  1. 21 CFR 212.20(e)Written QA procedures established, followed
  2. 21 CFR 212.50(d)Production area & equipment checks

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Precision Nuclear of Virginia, LLC

2
DateClassificationOfficeProject area
November 19, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 27, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Precision Nuclear of Virginia, LLC
  • FDA Inspection 960577 - 2015-11-19
  • FDA Inspection 820283 - 2013-02-27

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