Freespira, Inc.

Form 483

Kirkland, Washington, United StatesFEI 3010887638Issued October 10, 2017

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 3010887638.

Observations4

Issue DateOctober 10, 2017

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Freespira, Inc.
Location: Kirkland, Washington, United States
FEI Number: 3010887638
Product Type: Devices
Issue Date: October 10, 2017
Country: United States

Inspection History, 2017 to 2025

NAI1

VAI2

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

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Freespira, Inc. FDA Form 483, Kirkland, Washington, October 10, 2017