FDA inspection

Phelan Mfg Corp: FDA inspection ending Sep 28, 2015

FDA inspection 944644 · No Action Indicated (NAI) · Minneapolis, MN

Key facts

Inspection ID 944644
Firm Phelan Mfg Corp
FEI number 2126376
Address 2523 Minnehaha Ave
City Minneapolis
State MN
ZIP 55404
Country United States
Fiscal year 2015
Inspection end date Sep 28, 2015
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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