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FDA Inspection
•Delta Pharma, Inc.•June 2, 2023

FDA Inspection 1206930 - Delta Pharma, Inc. - June 02, 2023

Record Details

This FDA Inspection record concerns Delta Pharma, Inc., with an inspection on June 2, 2023, issued by the New Orleans District Office.

Company
Delta Pharma, Inc.
Inspection Date
June 2, 2023
Office
New Orleans District Office
People
  • Lareese K. Thomas (FDA Associated Person)
  • Sonya M. Edmonds (FDA Associated Person)
View Company Profile

ID · 1742a409-2a5d-4b11-aec6-e7765861703b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1206930
FDA center
Human Drugs
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.42(c)(10)(iv)Environmental Monitoring System

Full citation text and observation details available on the Dashboard.

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
May 20, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 23, 2017OAICenter 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 1169898 - 2022-05-20
  • FDA Inspection 1004804 - 2017-02-23
  • FDA Inspection 971348 - 2016-05-24

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