# Resonance Technology Inc - Inspection Records

Source: https://www.keypedia.com/companies/resonance-technology-inc/9fcf32e3-f685-4f84-b0f3-4b3910c9203f

> Inspection records and compliance data for Resonance Technology Inc in Northridge, California. Access full analysis and detailed observations.

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## Details

- Name: Resonance Technology Inc
- FEI Number: 1000306474
- City: Northridge
- State: California
- Country Name: United States
- Address Line 1: 18121 Parthenia St
- Zip Code: 91325

## Related Documents

- [483 - Resonance Technology Inc - 2025-10-17](https://www.keypedia.com/records/483/resonance-technology-inc/e6631620-1167-446e-ab6f-78a94f6bfd73) — source: FDA, date: October 17, 2025
- [FDA Inspection 1287668 - Resonance Technology Inc - 2025-10-17](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/52023835-eea8-409e-ad86-6c636904f214) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 17, 2025
- [FDA Inspection 1287668 - Resonance Technology Inc - 2025-10-17](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/19f9899a-f79e-4ae2-ad39-54e65b5a12c4) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2025
- [FDA Inspection 1287668 - Resonance Technology Inc - 2025-10-17](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/75a91a08-b52c-4838-8ecc-0d19d43d0d5a) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2025
- [FDA Inspection 1287668 - Resonance Technology Inc - 2025-10-17](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/48f0bd88-3557-4974-ac43-23ce0e1dd48d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 17, 2025
- [FDA Inspection 1181293 - Resonance Technology Inc - 2022-10-06](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/8f650356-910b-4e10-a6fc-8f5a01899816) — classification: No Action Indicated (NAI), source: FDA, date: October 6, 2022
- [FDA Inspection 1181293 - Resonance Technology Inc - 2022-10-06](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/2c54b89e-88fd-4b15-8fef-5a770af0109e) — classification: No Action Indicated (NAI), source: FDA, date: October 6, 2022
- [FDA Inspection 1099478 - Resonance Technology Inc - 2019-07-17](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/19871109-5954-454b-be22-ae0a262d9c8b) — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2019
- [FDA Inspection 1099478 - Resonance Technology Inc - 2019-07-17](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/3f328ac8-69d8-49a0-b141-4cabdc6edf57) — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2019
- [FDA Inspection 917272 - Resonance Technology Inc - 2015-02-20](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/4c078433-d01d-4122-9ada-05bc7d057ed1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 20, 2015
- [FDA Inspection 917272 - Resonance Technology Inc - 2015-02-20](https://www.keypedia.com/records/fda_inspections/resonance-technology-inc/d999dde2-af53-4151-a196-d3cfd6c7421d) — classification: No Action Indicated (NAI), source: FDA, date: February 20, 2015

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