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FDA Inspection 1326478 — Mark S. Denker, MD PA

Mark S. Denker, MD PA — FEI 3004450713

The FDA completed an inspection of Mark S. Denker, MD PA on July 14, 2026 in Boca Raton, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 14, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Boca Raton, FL (United States)

Facility

Other inspections at this facility

  • 1207527 (NAI Tue Jun 06 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1171177 (NAI Mon Jun 06 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 949687 (VAI Wed Nov 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 755670 (NAI Mon Dec 05 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 598743 (NAI Thu Jul 23 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources