# Symphony Inc - Inspection Records

Source: https://www.keypedia.com/companies/symphony-inc/c5886060-cc3b-4437-a056-1b7edab36c04

> Inspection records and compliance data for Symphony Inc in Moorestown, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Symphony Inc
- FEI Number: 1000122035
- City: Moorestown
- State: New Jersey
- Country Name: United States
- Address Line 1: 1263 Glen Ave Ste 220
- Zip Code: 08057

## Related Documents

- [FDA Inspection 1264162 - Symphony Inc - 2025-03-03](https://www.keypedia.com/records/fda_inspections/symphony-inc/27d14149-54c0-4348-9529-881ca704444b) — source: FDA, date: March 3, 2025
- [FDA Inspection 1264162 - Symphony Inc - 2025-03-03](https://www.keypedia.com/records/fda_inspections/symphony-inc/349ffbce-47df-41c1-aad5-a5c699e7ab50) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2025
- [FDA Inspection 1264162 - Symphony Inc - 2025-03-03](https://www.keypedia.com/records/fda_inspections/symphony-inc/da1e4b03-25e4-4797-b83c-d6b43fe495bf) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2025
- [FDA Inspection 1080991 - Symphony Inc - 2018-11-19](https://www.keypedia.com/records/fda_inspections/symphony-inc/b9f111c2-3160-4463-87b8-76328ddaf251) — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2018
- [FDA Inspection 956415 - Symphony Inc - 2016-01-07](https://www.keypedia.com/records/fda_inspections/symphony-inc/1ccd071c-d1a9-4e9b-8732-85f75fc33786) — classification: No Action Indicated (NAI), source: FDA, date: January 7, 2016
- [FDA Inspection 749162 - Symphony Inc - 2011-10-13](https://www.keypedia.com/records/fda_inspections/symphony-inc/e6f2a872-ed50-43e0-9038-d9a2b0e9c3e9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 13, 2011
- [FDA Inspection 542080 - Symphony Inc - 2008-10-17](https://www.keypedia.com/records/fda_inspections/symphony-inc/5f074a7d-2766-491d-95e4-3f64d4be7a93) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2008

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