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FDA Inspection
•Ghiath M. Mikdadi, M.D.•April 27, 2026

Ghiath M. Mikdadi, M.D. – FDA Inspection, Apr 27, 2026

Record Details

This FDA Inspection record concerns Ghiath M. Mikdadi, M.D., with an inspection on April 27, 2026, issued by the New Orleans District Office, covering human drugs.

Company
Ghiath M. Mikdadi, M.D.
Inspection Date
April 27, 2026
Product Type
Human Drugs
Office
New Orleans District Office
Person
  • Dana M. Klimavicz (Company Rep)
View Company Profile

ID · a83da6e3-ff3e-40d6-ba91-a12f0f8af0db

Inspection Facts

Inspection number
1315788
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued, view the record

FDA Citations

1
  1. 21 CFR 312.60FD-1572, protocol compliance

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Ghiath M. Mikdadi, M.D.

1
DateClassificationOfficeProject area
November 6, 2015NAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Ghiath M. Mikdadi, M.D.
  • FDA Inspection 947825 - 2015-11-06

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