Nutek Orthopaedics, Inc.

Form 483

Fort Lauderdale, Florida, United StatesFEI 3005893246Issued January 04, 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 3005893246.

Observations5

Issue DateJanuary 04, 2018

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Nutek Orthopaedics, Inc.
Location: Fort Lauderdale, Florida, United States
FEI Number: 3005893246
Product Type: Devices
Issue Date: January 04, 2018
Country: United States

Inspection History, 2011 to 2024

NAI2

VAI3

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

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Nutek Orthopaedics, Inc. FDA Form 483, Fort Lauderdale, Florida, January 4, 2018