Arcoma North America, Inc.

Form 483

Laguna Hills, California, United StatesFEI 3005998708Issued September 11, 2014

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 3005998708.

Observations1

Issue DateSeptember 11, 2014

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Arcoma North America, Inc.
Location: Laguna Hills, California, United States
FEI Number: 3005998708
Product Type: Devices
Issue Date: September 11, 2014
Country: United States

Inspection History, 2009 to 2014

NAI2

VAI1

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

Act on This Form 483

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Arcoma North America, Inc. FDA Form 483, Laguna Hills, California, September 11, 2014