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Eurofins Biopharma Product Testing, Denmark A/S, Glostrup, Denmark – FDA Inspections

Inspection records and compliance data for Eurofins Biopharma Product Testing, Denmark A/S in Glostrup. 5 FDA inspections on record, last inspected May 17, 2023.

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Company Profile

This profile covers Eurofins Biopharma Product Testing, Denmark A/S based in Glostrup, Denmark.

FDA Inspection History

FDA inspections
5
OAI
0
VAI
3
NAI
2
Form 483s
0
Warning letters
0

First inspected May 12, 2009. Last inspected May 17, 2023.

Most cited issue areas

  • Complete test data included in records1 inspection
  • Computer control of master formula records1 inspection
  • Deviations from laboratory control requirements1 inspection

FDA inspections (5)

DateResultFDA center(s)Insp. #
May 17, 2023NAIHuman Drugs · Drug Quality Assurance1222906
June 22, 2016VAIHuman Drugs · Drug Quality Assurance976102
December 14, 2012VAIHuman Drugs · Drug Quality Assurance811362
March 30, 2012NAIHuman Drugs · Drug Quality Assurance780431
May 12, 2009VAIHuman Drugs · Drug Quality Assurance578807
FDA documents

No Form 483s, Warning Letters or EIRs on record.

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Company Information

Name

Eurofins Biopharma Product Testing, Denmark A/S

FEI Number

3006272083

Address

Ornebjergvej 1, Glostrup, Denmark

Country

Denmark

ID: b229d16c-8c5e-4288-9c41-ff6ea8ba3df5

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