Fivos, Inc.

Form 483

West Lebanon, New Hampshire, United StatesFEI 3008850288Issued August 04, 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 3008850288.

Observations2

Issue DateAugust 04, 2014

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Fivos, Inc.
Location: West Lebanon, New Hampshire, United States
FEI Number: 3008850288
Product Type: Devices
Issue Date: August 04, 2014
Country: United States

Inspection History, 2014 to 2019

NAI2

VAI1

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

Act on This Form 483

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Fivos, Inc. FDA Form 483, West Lebanon, New Hampshire, August 4, 2014