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FDA Inspection
•Lilly del Caribe, Inc.•February 17, 2023

Lilly del Caribe, Inc. – FDA Inspection, Feb 17, 2023

Record Details

This FDA Inspection record concerns Lilly del Caribe, Inc., with an inspection on February 17, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Lilly del Caribe, Inc.
Inspection Date
February 17, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Angelica M. Hernandez (Issuing Officer)
  • Jose F. Velez (Issuing Officer)
  • Marian E. Ramirez (Company Rep)
View Company Profile

ID · c2c92c4c-c540-4128-90a5-30550b167b83

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1198613
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Lilly del Caribe, Inc.

8
DateClassificationOfficeProject area
May 12, 2026Not classifiedSan Juan District Office
September 27, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 1, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 21, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 4, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 8 other inspections on the company page
Other documents for Lilly del Caribe, Inc.
  • FDA Inspection 1321482 - 2026-05-12
  • FDA Inspection 1069980 - 2018-09-27
  • FDA Inspection 974723 - 2016-06-01
  • FDA Inspection 868382 - 2014-02-21
  • FDA Inspection 776200 - 2012-04-04

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