Percussionaire Corporation

Form 483

Sandpoint, Idaho, United StatesFEI 1000524541Issued March 24, 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 1000524541.

Observations4

Issue DateMarch 24, 2017

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Percussionaire Corporation
Location: Sandpoint, Idaho, United States
FEI Number: 1000524541
Product Type: Devices
Issue Date: March 24, 2017
Country: United States

Inspection History, 2014 to 2024

NAI1

VAI3

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

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Percussionaire Corporation FDA Form 483, Sandpoint, Idaho, March 24, 2017