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FDA Inspection
•Beasley E. Robert, MD•July 21, 2025

Beasley E. Robert, MD – FDA Inspection, Jul 21, 2025

Record Details

This FDA Inspection record concerns Beasley E. Robert, MD, with an inspection on July 21, 2025, issued by the Florida District Office, covering medical devices & rad health.

Company
Beasley E. Robert, MD
Inspection Date
July 21, 2025
Product Type
Medical Devices & Rad Health
Office
Florida District Office
Person
  • Emily A. Baldwin (Company Rep)
View Company Profile

ID · cce9ad6b-3e96-4539-a333-8fd2f4c2a659

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1276117
FDA center
Medical Devices & Rad Health
Project area
Product Evaluation: Medical Devices
Outcome
Form 483 issued, view the record

FDA Citations

1
  1. 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Beasley E. Robert, MD

2
DateClassificationOfficeProject area
June 7, 2018NAICenter for Devices and Radiological HealthBioresearch Monitoring
June 13, 2014NAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Beasley E. Robert, MD
  • FDA Inspection 1055836 - 2018-06-07
  • FDA Inspection 884381 - 2014-06-13

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