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FDA Inspection
•EUGIA Pharma Specialities Limited•February 27, 2026

EUGIA Pharma Specialities Limited – FDA Inspection, Feb 27, 2026

Record Details

This FDA Inspection record concerns EUGIA Pharma Specialities Limited, with an inspection on February 27, 2026, issued by the Office of Inspections and Investigations, covering human drugs.

Company
EUGIA Pharma Specialities Limited
Inspection Date
February 27, 2026
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Joseph A. Piechocki (Issuing Officer)
  • Matthew B. Casale (FDA Associated Person)
View Company Profile

ID · 7df17aa7-6253-487f-94ca-41e6ec737792

Inspection Facts

Inspection number
1304662
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

4
  1. 21 CFR 211.113(b)Procedures for sterile drug products
  2. 21 CFR 211.113(b)Validation lacking for sterile drug products
  3. 21 CFR 211.160(b)Scientifically sound laboratory controls
  4. 21 CFR 211.192Investigations of discrepancies, failures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of EUGIA Pharma Specialities Limited

6
DateClassificationOfficeProject area
July 26, 2023NAIDrug Quality Assurance
November 25, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 28, 2019VAIOffice of Inspections and InvestigationsGeneric Drug Evaluation
June 8, 2018Not classifiedOffice of Inspections and Investigations
December 14, 2017Not classifiedOffice of Inspections and Investigations
View all 6 other inspections on the company page
Other documents for EUGIA Pharma Specialities Limited
  • FDA Inspection 1234157 - 2023-07-26
  • FDA Inspection 1234762 - 2022-11-25
  • FDA Inspection 1100694 - 2019-08-28
  • FDA Inspection 1057278 - 2018-06-08
  • FDA Inspection 1039097 - 2017-12-14

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