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FDA Inspection
•Novant Health Presbyterian Medical Center•August 25, 2017

Novant Health Presbyterian Medical Center – FDA Inspection, Aug 25, 2017

Record Details

This FDA Inspection record concerns Novant Health Presbyterian Medical Center, with an inspection on August 25, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Novant Health Presbyterian Medical Center
Inspection Date
August 25, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Brentley S. Pittman (Investigator)
View Company Profile

ID · bdafeb33-fb0d-474d-8c7a-b68bd1ca5214

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1023386
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 610.47(b)Lookback System [Consignee]

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Novant Health Presbyterian Medical Center

6
DateClassificationOfficeProject area
September 12, 2024Not classifiedAtlanta District Office
May 24, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 19, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 14, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 14, 2011NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Novant Health Presbyterian Medical Center
  • FDA Inspection 1249457 - 2024-09-12
  • FDA Inspection 1092723 - 2019-05-24
  • FDA Inspection 927016 - 2015-05-19
  • FDA Inspection 814376 - 2013-01-14
  • FDA Inspection 720828 - 2011-04-14

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