FDA inspection

Xtreem Pulse LLC: FDA inspection ending Jun 29, 2022

FDA inspection 1173093 · Voluntary Action Indicated (VAI) · New York, NY

Key facts

Inspection ID 1173093
Firm Xtreem Pulse LLC
FEI number 3012470925
Address 353 W 29th St Apt 3
City New York
State NY
ZIP 10001
Country United States
Fiscal year 2022
Inspection end date Jun 29, 2022
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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