FDA Inspection
Deirdre O. Hooper, M.D.Deirdre O. Hooper, M.D. – FDA Inspection, Sep 10, 2025
Record Details
This FDA Inspection record concerns Deirdre O. Hooper, M.D., with an inspection on September 10, 2025, issued by the New Orleans District Office, covering medical devices & rad health.
- Company
- Deirdre O. Hooper, M.D.
- Inspection Date
- September 10, 2025
- Product Type
- Medical Devices & Rad Health
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ID · 5fc35f78-ae66-4e58-ac96-69efad1773e2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1281081
- FDA center
- Medical Devices & Rad Health
- Project area
- Product Evaluation: Medical Devices
FDA Citations
1- 21 CFR 812.140(a)(3)Investigator's subject records inadequate
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Other FDA inspections of Deirdre O. Hooper, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 21, 2019 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Deirdre O. Hooper, M.D.
- FDA Inspection 1112299 - 2019-11-21
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