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FDA Inspection
•Biomedical Research Foundation of Northwest Louisiana•April 18, 2024

Biomedical Research Foundation of Northwest Louisiana – FDA Inspection, Apr 18, 2024

Record Details

This FDA Inspection record concerns Biomedical Research Foundation of Northwest Louisiana, with an inspection on April 18, 2024, issued by the New Orleans District Office, covering human drugs.

Company
Biomedical Research Foundation of Northwest Louisiana
Inspection Date
April 18, 2024
Product Type
Human Drugs
Office
New Orleans District Office
People
  • Laurie Nelson (Issuing Officer)
  • Saundrea A. Munroe (FDA Associated Person)
View Company Profile

ID · cb58d528-7922-4187-94c5-55571acaaa93

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1237238
FDA center
Human Drugs
Project area
Generic Drug Evaluation
Outcome
Form 483 issued

FDA Citations

5
  1. 21 CFR 212.20(d)Determination need for investigation
  2. 21 CFR 212.30(b)Equipment procedures
  3. 21 CFR 212.40(a)Suitable for intended use
  4. 21 CFR 212.50(a)Written control procedures
  5. 21 CFR 212.70(d)(3)Final dated signature

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Biomedical Research Foundation of Northwest Louisiana

2
DateClassificationOfficeProject area
April 1, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 16, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Biomedical Research Foundation of Northwest Louisiana
  • FDA Inspection 979734 - 2016-04-01
  • FDA Inspection 831846 - 2013-05-16

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