Penumbra Inc.

Form 483

Alameda, California, United StatesFEI 3005168196Issued July 15, 2015

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 3005168196.

Observations1

Issue DateJuly 15, 2015

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Penumbra Inc.
Location: Alameda, California, United States
FEI Number: 3005168196
Product Type: Devices
Issue Date: July 15, 2015
Country: United States

Inspection History, 2009 to 2021

NAI5

VAI4

OAI1

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

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Penumbra Inc. FDA Form 483, Alameda, California, July 15, 2015