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FDA Inspection
•Delta Pharma, Inc.•April 12, 2024

Delta Pharma, Inc. – FDA Inspection, Apr 12, 2024

Record Details

This FDA Inspection record concerns Delta Pharma, Inc., with an inspection on April 12, 2024, issued by the New Orleans District Office, covering human drugs.

Company
Delta Pharma, Inc.
Inspection Date
April 12, 2024
Product Type
Human Drugs
Office
New Orleans District Office
Person
  • Margaret M. Annes (FDA Associated Person)
View Company Profile

ID · 3856282d-e9b3-4734-bb19-f1f6b2ce916c

Inspection Facts

Inspection number
1235500
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 211.110(a)Written in-process control procedures
  2. 21 CFR 211.80(a)Written Procedures Not Followed
  3. 21 CFR 211.84(b)Representative Samples

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
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 1292232 - 2025-11-21
  • 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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