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Nutek Orthopaedics, Inc. Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed 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.

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Nutek Orthopaedics, Inc.

Fort Lauderdale, Florida, United States
Issue DateJanuary 04, 2018
FEI Number3005893246
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Nutek Orthopaedics, Inc. FDA Form 483, Fort Lauderdale, Florida, January 4, 2018