Koros USA, Inc.

Form 483

Moorpark, California, United StatesFEI 2023918Issued November 14, 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 2023918.

Observations12

Issue DateNovember 14, 2016

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Koros USA, Inc.
Location: Moorpark, California, United States
FEI Number: 2023918
Product Type: Devices
Issue Date: November 14, 2016
Country: United States

Inspection History, 2010 to 2024

NAI1

VAI4

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

Act on This Form 483

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Koros USA, Inc. FDA Form 483, Moorpark, California, November 14, 2016