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FDA Inspection
•LGM Pharma Solutions, LLC•May 18, 2026

LGM Pharma Solutions, LLC – FDA Inspection, May 18, 2026

Record Details

This FDA Inspection record concerns LGM Pharma Solutions, LLC, with an inspection on May 18, 2026, issued by the Los Angeles District Office, covering human drugs.

Company
LGM Pharma Solutions, LLC
Inspection Date
May 18, 2026
Product Type
Human Drugs
Office
Los Angeles District Office
People
  • Devisree P. Mattigiri (Issuing Officer)
  • Jay-Ar C. Bendo (Issuing Officer)
  • Journey V Cordero (Issuing Officer)
  • Thuy Tram L. Nguyen (Issuing Officer)
  • Walden H. Lee (FDA Associated Person)
View Company Profile

ID · 862f3c9a-5369-473a-b4fe-259a971eb45c

Inspection Facts

Inspection number
1317740
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

4
  1. 21 CFR 211.100(a)Absence of Written Procedures
  2. 21 CFR 211.160(b)Scientifically sound laboratory controls
  3. 21 CFR 211.170(b)Annual visual exams of drug products
  4. 21 CFR 211.192Investigations of discrepancies, failures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of LGM Pharma Solutions, LLC

13
DateClassificationOfficeProject area
January 24, 2025NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
March 1, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 31, 2020NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 17, 2018VAICenter for Drug Evaluation and ResearchPostmarket Surv. and Epidemiology
October 20, 2017Not classifiedLos Angeles District OfficeGeneric Drug Evaluation
View all 13 other inspections on the company page
Other documents for LGM Pharma Solutions, LLC
  • FDA Inspection 1232056 - 2025-01-24
  • FDA Inspection 1230374 - 2024-03-01
  • FDA Inspection 1120565 - 2020-01-31
  • FDA Inspection 1062404 - 2018-08-17
  • FDA Inspection 1029466 - 2017-10-20

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