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FDA Inspection
•Delta Pharma, Inc.•November 21, 2025

FDA Inspection 1292232 - Delta Pharma, Inc. - November 21, 2025

Record Details

This FDA Inspection record concerns Delta Pharma, Inc., with an inspection on November 21, 2025, issued by the New Orleans District Office, covering human drugs.

Company
Delta Pharma, Inc.
Inspection Date
November 21, 2025
Product Type
Human Drugs
Office
New Orleans District Office
Person
  • Jared P. Stevens (FDA Associated Person)
View Company Profile

ID · 80d920f8-4805-4a4a-bd47-6f597d08fdc2

Inspection Facts

Inspection number
1292232
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.87Retest of approved components/containers/closures
  2. FDCA 503B(a)(10)(A)Drug product labels, fails to include

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Delta Pharma, Inc.

7
DateClassificationOfficeProject area
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
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 1235500 - 2024-04-12
  • FDA Inspection 1206930 - 2023-06-02
  • FDA Inspection 1169898 - 2022-05-20
  • FDA Inspection 1004804 - 2017-02-23
  • FDA Inspection 971348 - 2016-05-24

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