FDA inspection

Pro-Tech Design & Manufacturing, Inc.: FDA inspection ending Jun 12, 2014

FDA inspection 886604 · Voluntary Action Indicated (VAI) · Santa Fe Springs, CA

Key facts

Inspection ID 886604
Firm Pro-Tech Design & Manufacturing, Inc.
FEI number 3003574398
Address 14561 Marquardt Ave
City Santa Fe Springs
State CA
ZIP 90670
Country United States
Fiscal year 2014
Inspection end date Jun 12, 2014
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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