FDA inspection

MOXI Enterprises LLC: FDA inspection ending Dec 14, 2010

FDA inspection 701633 · No Action Indicated (NAI) · Greenville, SC

Key facts

Inspection ID 701633
Firm MOXI Enterprises LLC
FEI number 3008146946
Address 1939 S Vandeventer Ave
City Greenville
State SC
ZIP 29605
Country United States
Fiscal year 2011
Inspection end date Dec 14, 2010
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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