FDA inspection

Remel Atlanta, A Div. of Remel, Inc.: FDA inspection ending Nov 19, 2013

FDA inspection 858436 · No Action Indicated (NAI) · Norcross, GA

Key facts

Inspection ID 858436
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 2014
Inspection end date Nov 19, 2013
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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