FDA inspection

Evans Manufacturing: FDA inspection ending Oct 11, 2018

FDA inspection 1069494 · Voluntary Action Indicated (VAI) · Garden Grove, CA

Key facts

Inspection ID 1069494
Firm Evans Manufacturing
FEI number 1000340275
Address 7422 Chapman Ave
City Garden Grove
State CA
ZIP 92841
Country United States
Fiscal year 2019
Inspection end date Oct 11, 2018
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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