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FDA Inspection
•Eurofins SF Analytical Laboratories, Inc.•June 3, 2026

Eurofins SF Analytical Laboratories, Inc. – FDA Inspection, Jun 3, 2026

Record Details

This FDA Inspection record concerns Eurofins SF Analytical Laboratories, Inc., with an inspection on June 3, 2026, issued by the Philadelphia District Office, covering human drugs.

Company
Eurofins SF Analytical Laboratories, Inc.
Inspection Date
June 3, 2026
Product Type
Human Drugs
Office
Philadelphia District Office
Person
  • Pushpa S. Jayasekara (FDA Associated Person)
View Company Profile

ID · 37efefb1-8039-486d-b5cd-3818f492c05a

Inspection Facts

Inspection number
1321212
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

5
  1. 21 CFR 211.160(b)Scientifically sound laboratory controls
  2. 21 CFR 211.192Investigations of discrepancies, failures
  3. 21 CFR 211.194(a)(4)Complete Test Data
  4. 21 CFR 211.194(a)(8)Second person sign off
  5. 21 CFR 211.68(b)Computer control of master formula records

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Eurofins SF Analytical Laboratories, Inc.

3
DateClassificationOfficeProject area
August 9, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 22, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 27, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Eurofins SF Analytical Laboratories, Inc.
  • FDA Inspection 1177148 - 2022-08-09
  • FDA Inspection 911124 - 2015-01-22
  • FDA Inspection 736116 - 2011-07-27

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