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FDA Inspection
•Murtaza Mussaji, D.O..•August 28, 2026

Murtaza Mussaji, D.O.. – FDA Inspection, Aug 28, 2026

Record Details

This FDA Inspection record concerns Murtaza Mussaji, D.O.., with an inspection on August 28, 2026, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Murtaza Mussaji, D.O..
Inspection Date
August 28, 2026
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Ruth E. Medcalf (Issuing Officer)
View Company Profile

ID · 2b935b38-6786-4788-99d1-9f8c1428f865

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1333738
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 Murtaza Mussaji, D.O..

1
DateClassificationOfficeProject area
August 16, 2022VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Murtaza Mussaji, D.O..
  • FDA Inspection 1178687 - 2022-08-16

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