# Beacon Converters, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/beacon-converters-inc/c3c3c4f7-e0c9-41f0-8cf8-e18b4f0b00a0

> Inspection records and compliance data for Beacon Converters, Inc. in Saddle Brook, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Beacon Converters, Inc.
- FEI Number: 2242794
- City: Saddle Brook
- State: New Jersey
- Country Name: United States
- Address Line 1: Andrea Blvd., Bldg. P1
- Zip Code: 07663

## Related Documents

- [FDA Inspection 985052 - Beacon Converters, Inc. - 2016-09-13](https://www.globalkeysolutions.net/records/fda_inspections/beacon-converters-inc/d5ae40df-9796-4f93-a3ab-ef1b0e9eb29a) — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2016
- [FDA Inspection 985052 - Beacon Converters, Inc. - 2016-09-13](https://www.globalkeysolutions.net/records/fda_inspections/beacon-converters-inc/95d0bc94-3fbf-42f0-9ae9-8f88a1d4a979) — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2016
- [FDA Inspection 791148 - Beacon Converters, Inc. - 2012-06-21](https://www.globalkeysolutions.net/records/fda_inspections/beacon-converters-inc/6713bf99-2651-44c4-8f22-3ddfca8cffd6) — classification: No Action Indicated (NAI), source: FDA, date: June 21, 2012
- [FDA Inspection 791148 - Beacon Converters, Inc. - 2012-06-21](https://www.globalkeysolutions.net/records/fda_inspections/beacon-converters-inc/328f37be-afb9-4cd9-9be6-35f0102238e6) — classification: No Action Indicated (NAI), source: FDA, date: June 21, 2012
- [FDA Inspection 576573 - Beacon Converters, Inc. - 2009-04-15](https://www.globalkeysolutions.net/records/fda_inspections/beacon-converters-inc/581bc368-222e-4c7c-b585-9a0c1ff47ff9) — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2009
- [FDA Inspection 576573 - Beacon Converters, Inc. - 2009-04-15](https://www.globalkeysolutions.net/records/fda_inspections/beacon-converters-inc/b1c82619-2952-4b05-9071-dbcaee7baadf) — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2009

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