FDA inspection

Aprios Custom Mfg: FDA inspection ending Mar 30, 2022

FDA inspection 1166867 · No Action Indicated (NAI) · Minneapolis, MN

Key facts

Inspection ID 1166867
Firm Aprios Custom Mfg
FEI number 3004612223
Address 8617 Xylon Ct
City Minneapolis
State MN
ZIP 55445
Country United States
Fiscal year 2022
Inspection end date Mar 30, 2022
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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