K2M, Inc.

Form 483

Leesburg, Virginia, United StatesFEI 3008599177Issued November 16, 2016

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3008599177.

Observations2

Issue DateNovember 16, 2016

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: K2M, Inc.
Location: Leesburg, Virginia, United States
FEI Number: 3008599177
Product Type: Devices
Issue Date: November 16, 2016
Country: United States

Inspection History, 2011 to 2024

NAI8

VAI2

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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K2M, Inc. FDA Form 483, Leesburg, Virginia, November 16, 2016