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FDA Inspection
•Galephar Pharmaceutical Research Inc.•October 24, 2018

Galephar Pharmaceutical Research Inc. – FDA Inspection, Oct 24, 2018

Record Details

This FDA Inspection record concerns Galephar Pharmaceutical Research Inc., with an inspection on October 24, 2018, issued by the San Juan District Office, covering human drugs.

Company
Galephar Pharmaceutical Research Inc.
Inspection Date
October 24, 2018
Product Type
Human Drugs
Office
San Juan District Office
Person
  • Libia M. Lugo (Issuing Officer)
View Company Profile

ID · fe3b003c-59d4-4924-84d5-ce168fe9986a

Inspection Facts

Inspection number
1069913
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Galephar Pharmaceutical Research Inc.

6
DateClassificationOfficeProject area
October 18, 2024VAISan Juan District OfficeDrug Quality Assurance
November 23, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 29, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 4, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 30, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Galephar Pharmaceutical Research Inc.
  • FDA Inspection 1252181 - 2024-10-18
  • FDA Inspection 952658 - 2015-11-23
  • FDA Inspection 747557 - 2011-09-29
  • FDA Inspection 667983 - 2010-06-04
  • FDA Inspection 559310 - 2009-01-30

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