ReNovo, Inc.

Form 483FOIA Uncovered

Bend, OregonFEI 3014023545Issued June 21, 2018

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 3014023545.

ObservationsNot available

Issue DateJune 21, 2018

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: ReNovo, Inc.
Location: Bend, Oregon
FEI Number: 3014023545
Product Type: Devices
Issue Date: June 21, 2018
Country: United States

Inspection History, 2018 to 2023

VAI1

OAI1

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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ReNovo, Inc. FDA Form 483, Bend, Oregon, June 21, 2018