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FDA Inspection
•Cooperman Barnabas Medical Center Inc•November 7, 2014

Cooperman Barnabas Medical Center Inc – FDA Inspection, Nov 7, 2014

Record Details

This FDA Inspection record concerns Cooperman Barnabas Medical Center Inc, with an inspection on November 7, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Cooperman Barnabas Medical Center Inc
Inspection Date
November 7, 2014
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 32384c8f-f86a-47c9-b9be-d4cc2a3bf677

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
903748
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.60(a)Equipment observed, standardized, calibrated

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Cooperman Barnabas Medical Center Inc

7
DateClassificationOfficeProject area
June 2, 2025NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 20, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 12, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 11, 2017Not classifiedNew Jersey District Office
April 29, 2013VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for Cooperman Barnabas Medical Center Inc
  • FDA Inspection 1271693 - 2025-06-02
  • FDA Inspection 1203599 - 2023-04-20
  • FDA Inspection 1102095 - 2019-09-12
  • FDA Inspection 1013996 - 2017-05-11
  • FDA Inspection 829353 - 2013-04-29

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