FDA inspection

DERMACLIP US, LLC: FDA inspection ending Mar 2, 2017

FDA inspection 1020994 · Voluntary Action Indicated (VAI) · Houston, TX

Key facts

Inspection ID 1020994
Firm DERMACLIP US, LLC
FEI number 3011656357
Address 730 N Post Oak Rd Ste 202
City Houston
State TX
ZIP 77024
Country United States
Fiscal year 2017
Inspection end date Mar 2, 2017
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No 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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