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FDA Inspection
•OHM Pharma, Inc.•May 23, 2019

OHM Pharma, Inc. – FDA Inspection, May 23, 2019

Record Details

This FDA Inspection record concerns OHM Pharma, Inc., with an inspection on May 23, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
OHM Pharma, Inc.
Inspection Date
May 23, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Noreen Muniz (FDA Associated Person)
View Company Profile

ID · 8a5a0996-5966-4654-b684-f50c455dcdc2

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1092794
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued
Enforcement
Warning Letter

Other FDA inspections of OHM Pharma, Inc.

7
DateClassificationOfficeProject area
April 29, 2025Not classifiedDallas District Office
March 28, 2024VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
July 29, 2022NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
November 19, 2021NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 18, 2020VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
View all 7 other inspections on the company page
Other documents for OHM Pharma, Inc.
  • FDA Inspection 1230059 - 2025-04-29
  • FDA Inspection 1230961 - 2024-03-28
  • FDA Inspection 1175965 - 2022-07-29
  • FDA Inspection 1158974 - 2021-11-19
  • FDA Inspection 1122710 - 2020-03-18

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