# Nemcomed FW LLC dba Avalign Instruments and Implants - Inspection Records

Source: https://www.keypedia.com/companies/nemcomed-fw-llc-dba-avalign-instruments-and-implants/b0758b28-0d1f-43f5-a1bd-7a8112a5215d

> Inspection records and compliance data for Nemcomed FW LLC dba Avalign Instruments and Implants in Fort Wayne, Indiana. Access full analysis and detailed observations.

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## Details

- Name: Nemcomed FW LLC dba Avalign Instruments and Implants
- FEI Number: 3006128100
- City: Fort Wayne
- State: Indiana
- Country Name: United States
- Address Line 1: 8727 Clinton Park Dr
- Zip Code: 46825

## Related Documents

- [483 - Nemcomed FW LLC dba Avalign Instruments and Implants - 2025-01-16](https://www.keypedia.com/records/483/nemcomed-fw-llc-dba-avalign-instruments-and-implants/68f517ce-80d9-494a-8f75-a70dd85a4085) — source: FDA, date: January 16, 2025
- [FDA Inspection 1251833 - Nemcomed FW LLC dba Avalign Instruments and Implants - 2025-01-16](https://www.keypedia.com/records/fda_inspections/nemcomed-fw-llc-dba-avalign-instruments-and-implants/c129aaa0-dc42-4fad-a4fe-c08d73f72e36) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 16, 2025
- [FDA Inspection 1251833 - Nemcomed FW LLC dba Avalign Instruments and Implants - 2025-01-16](https://www.keypedia.com/records/fda_inspections/nemcomed-fw-llc-dba-avalign-instruments-and-implants/bf074eb2-7fb8-47c1-b0f3-2bfb3fed9ce2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 16, 2025
- [FDA Inspection 1006636 - Nemcomed FW LLC dba Avalign Instruments and Implants - 2017-04-05](https://www.keypedia.com/records/fda_inspections/nemcomed-fw-llc-dba-avalign-instruments-and-implants/25cbe8b7-1036-4794-85f2-7139be3e889e) — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2017
- [FDA Inspection 1006636 - Nemcomed FW LLC dba Avalign Instruments and Implants - 2017-04-05](https://www.keypedia.com/records/fda_inspections/nemcomed-fw-llc-dba-avalign-instruments-and-implants/2951467a-1e69-42fa-9835-31bef4201a24) — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2017

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## Related Officers

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