Eurofins Biopharma Product Testing, Denmark A/S

Form 483

Glostrup, -, DenmarkFEI 3006272083Issued June 22, 2016

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3006272083.

Observations5

Issue DateJune 22, 2016

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Eurofins Biopharma Product Testing, Denmark A/S
Location: Glostrup, -, Denmark
FEI Number: 3006272083
Product Type: Drugs
Issue Date: June 22, 2016
Country: Denmark

Inspection History, 2009 to 2023

NAI2

VAI3

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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Eurofins Biopharma Product Testing, Denmark A/S FDA Form 483, Glostrup, June 22, 2016