FDA inspection

ImpactLife: FDA inspection ending Oct 18, 2018

FDA inspection 1069355 · No Action Indicated (NAI) · Muscatine, IA

Key facts

Inspection ID 1069355
Firm ImpactLife
FEI number 1937802
Address 2604 2nd Ave Ste 6
City Muscatine
State IA
ZIP 52761
Country United States
Fiscal year 2019
Inspection end date Oct 18, 2018
Classification No Action Indicated (NAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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