FDA inspection

Poiesis Medical, LLC: FDA inspection ending Jan 30, 2019

FDA inspection 1078304 · Voluntary Action Indicated (VAI) · Jupiter, FL

Key facts

Inspection ID 1078304
Firm Poiesis Medical, LLC
FEI number 3009425008
Address 1095 Jupiter Commerce Pk Unit 10
City Jupiter
State FL
ZIP 33458
Country United States
Fiscal year 2019
Inspection end date Jan 30, 2019
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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