# Nutek Orthopaedics, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/nutek-orthopaedics-inc/fe93f8bb-c176-4700-b8e2-47e32ba4da78

> Inspection records and compliance data for Nutek Orthopaedics, Inc. in Fort Lauderdale, Florida. Access full analysis and detailed observations.

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## Details

- Name: Nutek Orthopaedics, Inc.
- FEI Number: 3005893246
- City: Fort Lauderdale
- State: Florida
- Country Name: United States
- Address Line 1: 641 SW 3rd Ave
- Zip Code: 33315

## Related Documents

- [483 - Nutek Orthopaedics, Inc. - 2024-11-19](https://www.keypedia.com/records/483/nutek-orthopaedics-inc/7c349910-ab1d-412c-b449-d808ffadd305) — source: FDA, date: November 19, 2024
- [FDA Inspection 1254551 - Nutek Orthopaedics, Inc. - 2024-11-19](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/6f009421-4db4-480e-ba42-90c106fc9159) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 19, 2024
- [FDA Inspection 1254551 - Nutek Orthopaedics, Inc. - 2024-11-19](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/3b8e9a81-0371-4ced-aca8-4053ecc765ad) — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2024
- [FDA Inspection 1254551 - Nutek Orthopaedics, Inc. - 2024-11-19](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/f75a7c14-8900-43fd-9522-eff03c20d99c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 19, 2024
- [FDA Inspection 1254551 - Nutek Orthopaedics, Inc. - 2024-11-19](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/3fbc3408-85e8-4e11-aedf-5839e96210e4) — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2024
- [FDA Inspection 1199695 - Nutek Orthopaedics, Inc. - 2023-03-09](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/0f722c4a-3497-441b-84e6-5d71255620d1) — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2023
- [FDA Inspection 1199695 - Nutek Orthopaedics, Inc. - 2023-03-09](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/6f873e81-71fb-40ea-923b-14c3bc95ec3c) — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2023
- [FDA Inspection 1036749 - Nutek Orthopaedics, Inc. - 2018-01-04](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/194cd264-a3f1-49e2-b632-5e5f544b308c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 4, 2018
- [FDA Inspection 1036749 - Nutek Orthopaedics, Inc. - 2018-01-04](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/66d3c140-b96f-4787-992d-fc8ab2c951f9) — classification: No Action Indicated (NAI), source: FDA, date: January 4, 2018
- [FDA Inspection 895261 - Nutek Orthopaedics, Inc. - 2014-09-12](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/96940845-d43c-4bb4-ad44-80ac7f07d3c5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 12, 2014
- [FDA Inspection 753056 - Nutek Orthopaedics, Inc. - 2011-11-04](https://www.keypedia.com/records/fda_inspections/nutek-orthopaedics-inc/de3a825f-69d3-4ed3-b50d-76b6769605bb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 4, 2011

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