# G.P. De Silva Spices, Inc. (DBA Grupo Canela), Pico Rivera, CA – FDA Inspections

Source: https://www.keypedia.com/companies/gp-de-silva-spices-inc-dba-grupo-canela/2b383296-d97e-428f-96c9-959be69bc49a

> Inspection records and compliance data for G.P. De Silva Spices, Inc. (DBA Grupo Canela) in Pico Rivera, California. 5 FDA inspections on record, 1 Form 483, last inspected June 02, 2026.

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## Details

- Name: G.P. De Silva Spices, Inc. (DBA Grupo Canela)
- FEI Number: 3003441180
- Address Line 1: 8531 Loch Lomond Dr
- City: Pico Rivera
- State: California
- Zip Code: 90660
- Country Name: United States
- Address: 8531 Loch Lomond Dr, Pico Rivera, California 90660, United States
- Country: United States

## Related Documents

- FDA Inspection 1321758 - G.P. De Silva Spices, Inc. (DBA Grupo Canela) - 2026-06-02 — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2026
- FDA Inspection 1255288 - G.P. De Silva Spices, Inc. (DBA Grupo Canela) - 2024-12-11 — source: FDA, date: December 11, 2024
- FDA Inspection 1255288 - G.P. De Silva Spices, Inc. (DBA Grupo Canela) - 2024-12-11 — classification: No Action Indicated (NAI), source: FDA, date: December 11, 2024
- [FDA Inspection 1255288 - G.P. De Silva Spices, Inc. (DBA Grupo Canela) - 2024-12-11](https://www.keypedia.com/records/fda_inspections/gp-de-silva-spices-inc-dba-grupo-canela/d5514f80-e7bf-4ab5-82b2-b02e2af3e969) — classification: No Action Indicated (NAI), source: FDA, date: December 11, 2024
- FDA Inspection 1140905 - G.P. De Silva Spices, Inc. (DBA Grupo Canela) - 2021-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2021
- [FDA Inspection 1064605 - G.P. De Silva Spices, Inc. (DBA Grupo Canela) - 2018-09-04](https://www.keypedia.com/records/fda_inspections/gp-de-silva-spices-inc-dba-grupo-canela/53749886-ec1d-4ff0-9ded-fb3fe69a71c0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 4, 2018
- FDA Inspection 973840 - G.P. De Silva Spices, Inc. (DBA Grupo Canela) - 2016-06-07 — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2016

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