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FDA Inspection
•Medline Industries Inc•June 21, 2012

Medline Industries Inc – FDA Inspection, Jun 21, 2012

Record Details

This FDA Inspection record concerns Medline Industries Inc, with an inspection on June 21, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Medline Industries Inc
Inspection Date
June 21, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 156ae3f1-2ac8-4c27-a108-7a3892a54287

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
791750
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

2
  1. 21 CFR 211.100(b)Procedure Deviations Recorded and Justified
  2. 21 CFR 211.192Extent of discrepancy, failure investigations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Medline Industries Inc

4
DateClassificationOfficeProject area
March 11, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
August 2, 2013VAICenter for Devices and Radiological HealthProject Evaluation: Devices
July 20, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 25, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Medline Industries Inc
  • FDA Inspection 913527 - 2015-03-11
  • FDA Inspection 842504 - 2013-08-02
  • FDA Inspection 739871 - 2011-07-20
  • FDA Inspection 614934 - 2009-09-25

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