# Spectra Medical Devices, Llc - Inspection Records

Source: https://www.keypedia.com/companies/spectra-medical-devices-llc/26b1d6e1-5a34-438c-a935-dde37cfd3885

> Inspection records and compliance data for Spectra Medical Devices, Llc in Wilmington, Massachusetts. Access full analysis and detailed observations.

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## Details

- Name: Spectra Medical Devices, Llc
- FEI Number: 3000204727
- City: Wilmington
- State: Massachusetts
- Country Name: United States
- Address Line 1: 299 Ballardvale St Ste 1
- Zip Code: 01887

## Related Documents

- [FDA Inspection 1237163 - Spectra Medical Devices, Llc - 2024-04-25](https://www.keypedia.com/records/fda_inspections/spectra-medical-devices-llc/83a29ade-eceb-41ad-81bf-5574e01aef2a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 25, 2024
- [FDA Inspection 1237163 - Spectra Medical Devices, Llc - 2024-04-25](https://www.keypedia.com/records/fda_inspections/spectra-medical-devices-llc/fa18cc5c-6585-4fd6-9dc1-5a515a7259ab) — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2024
- [FDA Inspection 1007007 - Spectra Medical Devices, Llc - 2017-03-30](https://www.keypedia.com/records/fda_inspections/spectra-medical-devices-llc/fe454525-5f9d-43ca-b33e-4d81f0663a36) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 30, 2017
- [FDA Inspection 1007007 - Spectra Medical Devices, Llc - 2017-03-30](https://www.keypedia.com/records/fda_inspections/spectra-medical-devices-llc/a5578aa0-f6b2-4039-8398-a0d699c34a55) — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2017
- [FDA Inspection 779912 - Spectra Medical Devices, Llc - 2012-05-04](https://www.keypedia.com/records/fda_inspections/spectra-medical-devices-llc/6d419a7c-019c-4a18-a206-0ffd95faa192) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 4, 2012
- [FDA Inspection 779912 - Spectra Medical Devices, Llc - 2012-05-04](https://www.keypedia.com/records/fda_inspections/spectra-medical-devices-llc/f2ceefce-28cd-43f8-acd1-4c9ac133db0a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 4, 2012

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