FDA inspection

Poiesis Medical, LLC: FDA inspection ending May 22, 2017

FDA inspection 1012583 · Voluntary Action Indicated (VAI) · Jupiter, FL

Key facts

Inspection ID 1012583
Firm Poiesis Medical, LLC
FEI number 3009425008
Address 151 Fern St Ste 1
City Jupiter
State FL
ZIP 33458
Country United States
Fiscal year 2017
Inspection end date May 22, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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