FDA inspection

Richmond Products Inc.: FDA inspection ending Oct 29, 2015

FDA inspection 947844 · No Action Indicated (NAI) · Albuquerque, NM

Key facts

Inspection ID 947844
Firm Richmond Products Inc.
FEI number 1035253
Address 4400 Silver Ave SE
City Albuquerque
State NM
ZIP 87108
Country United States
Fiscal year 2016
Inspection end date Oct 29, 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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