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483
•Kimberly P. Cockerham, MD•June 3, 2026

Kimberly P. Cockerham, MD – FDA 483, Jun 3, 2026

Record Details

An FDA inspection of Kimberly P. Cockerham, MD in Wildwood, FL, revealed significant deviations in the conduct of a clinical investigation. The firm failed to adhere to the signed statement of investigator and investigational plan, including administering investigational product to a subject who met exclusion criteria and after unreported temperature excursions. Additionally, sponsor-provided visual acuity worksheets were not utilized for all randomized subjects.

Company
Kimberly P. Cockerham, MD
Inspection date
June 3, 2026
Product type
drugs
Office
Office of Medical Device and Radiological Health Division II
Person
  • Emily A. Baldwin (investigator)
View Company Profile

ID · 5def710f-ce20-429e-ba6d-9f287740658a

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