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FDA Inspection
•Delta Pharma, Inc.•February 23, 2017

Delta Pharma, Inc. – FDA Inspection, Feb 23, 2017

Record Details

This FDA Inspection record concerns Delta Pharma, Inc., with an inspection on February 23, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Delta Pharma, Inc.
Inspection Date
February 23, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Brandon C. Heitmeier (FDA Associated Person)
  • Diane P. Goyette (FDA Associated Person)
  • Shelby N. Turner (Investigator)
View Company Profile

ID · 734f2b2a-b199-48d2-8e52-c626e2160842

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
1004804
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Delta Pharma, Inc.

7
DateClassificationOfficeProject area
November 21, 2025Not classifiedNew Orleans District OfficeDrug Quality Assurance
April 12, 2024Not classifiedNew Orleans District OfficeDrug Quality Assurance
June 2, 2023VAINew Orleans District Office
May 20, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 24, 2016OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Delta Pharma, Inc.
  • FDA Inspection 1292232 - 2025-11-21
  • FDA Inspection 1235500 - 2024-04-12
  • FDA Inspection 1206930 - 2023-06-02
  • FDA Inspection 1169898 - 2022-05-20
  • FDA Inspection 971348 - 2016-05-24

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