# FDA Inspection 1281081 - Deirdre O. Hooper, M.D. - September 10, 2025

Source: https://www.keypedia.com/records/fda_inspections/deirdre-o-hooper-md/5fc35f78-ae66-4e58-ac96-69efad1773e2
Source feed: FDA_Inspections

> FDA Inspection 1281081 for Deirdre O. Hooper, M.D. on September 10, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1281081
- Company Name: Deirdre O. Hooper, M.D.
- Inspection Date: 2025-09-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New Orleans District Office

## Related Documents

- [FDA Inspection 1281081 - 2025-09-10](https://www.keypedia.com/records/fda_inspections/deirdre-o-hooper-md/f290946b-603a-4b1e-9e08-ec4338f0cba4)
- [FDA Inspection 1112299 - 2019-11-21](https://www.keypedia.com/records/fda_inspections/deirdre-o-hooper-md/8b28f01b-4dd0-4906-941e-eae3184103dc)

Company: https://www.keypedia.com/companies/deirdre-o-hooper-md/66497ec3-68f2-40b7-9b6a-703d333737c7

Office: https://www.keypedia.com/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea