Respicardia, Inc.

Form 483

Minnetonka, Minnesota, United StatesFEI 3009144177Issued February 13, 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 3009144177.

Observations1

Issue DateFebruary 13, 2017

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Respicardia, Inc.
Location: Minnetonka, Minnesota, United States
FEI Number: 3009144177
Product Type: Devices
Issue Date: February 13, 2017
Country: United States

Inspection History, 2015 to 2024

NAI2

VAI1

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

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Respicardia, Inc. FDA Form 483, Minnetonka, Minnesota, February 13, 2017