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FDA Inspection
•U.S. Dept. of Veterans Affairs, Northport VA Medical Center•February 1, 2013

U.S. Dept. of Veterans Affairs, Northport VA Medical Center – FDA Inspection, Feb 1, 2013

Record Details

This FDA Inspection record concerns U.S. Dept. of Veterans Affairs, Northport VA Medical Center, with an inspection on February 1, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
U.S. Dept. of Veterans Affairs, Northport VA Medical Center
Inspection Date
February 1, 2013
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · e45ef724-9c8b-4eb0-a389-7bc8ea6d41b2

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
816288
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

4
  1. 21 CFR 606.160(b)Required records
  2. 21 CFR 606.160(a)(1)Concurrent documentation
  3. 21 CFR 606.160(a)(1)Person performing, test results, interpretation
  4. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

Full citation text and observation details available on the Dashboard.

Other FDA inspections of U.S. Dept. of Veterans Affairs, Northport VA Medical Center

8
DateClassificationOfficeProject area
September 3, 2026Not classifiedNew York District OfficeBlood and Blood Products
January 9, 2024VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 18, 2021VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 26, 2018VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 12, 2016VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 8 other inspections on the company page
Other documents for U.S. Dept. of Veterans Affairs, Northport VA Medical Center
  • FDA Inspection 1334788 - 2026-09-03
  • FDA Inspection 1226814 - 2024-01-09
  • FDA Inspection 1142154 - 2021-05-18
  • FDA Inspection 1039133 - 2018-01-26
  • FDA Inspection 980282 - 2016-08-12

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