FDA inspection

Remel Atlanta, A Div. of Remel, Inc.: FDA inspection ending Apr 19, 2017

FDA inspection 1017035 · No Action Indicated (NAI) · Norcross, GA

Key facts

Inspection ID 1017035
Firm Remel Atlanta, A Div. of Remel, Inc.
FEI number 1031428
Address 2797 Peterson Pl
City Norcross
State GA
ZIP 30071
Country United States
Fiscal year 2017
Inspection end date Apr 19, 2017
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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