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FDA Inspection
•UBI Pharma, Inc.•June 20, 2019

UBI Pharma, Inc. – FDA Inspection, Jun 20, 2019

Record Details

This FDA Inspection record concerns UBI Pharma, Inc., with an inspection on June 20, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
UBI Pharma, Inc.
Inspection Date
June 20, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • David J. Gomes (Issuing Officer)
  • Kham Phommachanh (FDA Associated Person)
View Company Profile

ID · df85d9ee-ae80-49ae-b430-d7efd7d8a70d

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1095285
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of UBI Pharma, Inc.

6
DateClassificationOfficeProject area
October 14, 2025Not classifiedOffice of Inspections and Investigations
June 6, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 21, 2018Not classifiedOffice of Inspections and Investigations
May 4, 2018Not classifiedOffice of Inspections and Investigations
July 18, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for UBI Pharma, Inc.
  • FDA Inspection 1290852 - 2025-10-14
  • FDA Inspection 1207579 - 2023-06-06
  • FDA Inspection 1078315 - 2018-12-21
  • FDA Inspection 1052235 - 2018-05-04
  • FDA Inspection 890363 - 2014-07-18

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