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FDA Inspection
•Laboratorios Liconsa SAU•July 9, 2026

Laboratorios Liconsa SAU – FDA Inspection, Jul 9, 2026

Record Details

This FDA Inspection record concerns Laboratorios Liconsa SAU, with an inspection on July 9, 2026, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Laboratorios Liconsa SAU
Inspection Date
July 9, 2026
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Chad W. Rice (Company Rep)
View Company Profile

ID · 5cc57644-a02c-4548-80f8-5253527d3832

Inspection Facts

Inspection number
1325076
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.170(b)Investigation of reserve sample deterioration
  2. 21 CFR 211.192Investigations of discrepancies, failures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Laboratorios Liconsa SAU

8
DateClassificationOfficeProject area
January 17, 2025Not classifiedOffice of Inspections and Investigations
April 19, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 22, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 22, 2019Not classifiedOffice of Inspections and Investigations
September 15, 2017Not classifiedOffice of Inspections and Investigations
View all 8 other inspections on the company page
Other documents for Laboratorios Liconsa SAU
  • FDA Inspection 1251910 - 2025-01-17
  • FDA Inspection 1279060 - 2023-04-19
  • FDA Inspection 1136711 - 2019-03-22
  • FDA Inspection 1085151 - 2019-02-22
  • FDA Inspection 1029229 - 2017-09-15

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