FDA inspection

Advance-Esthetic LLC: FDA inspection ending Nov 6, 2025

FDA inspection 1280825 · Fort Lauderdale, FL

Key facts

Inspection ID 1280825
Firm Advance-Esthetic LLC
FEI number 3013397886
Address 4101 Ravenswood Rd Ste 110
City Fort Lauderdale
State FL
ZIP 33312-5371
Fiscal year 2026
Inspection end date Nov 6, 2025
Project area Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority
Product type Devices
Warning letter 729267

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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