# Strings Restaurant Group, Rancho Cordova, CA – FDA Inspections

Source: https://www.keypedia.com/companies/strings-restaurant-group/6654ea89-9804-4691-910b-c5b8c845741c

> Inspection records and compliance data for Strings Restaurant Group in Rancho Cordova, California. 5 FDA inspections on record, last inspected July 25, 2023.

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## Details

- Name: Strings Restaurant Group
- FEI Number: 3000203392
- Address Line 1: 11437 Sunrise Gold Cir Ste C
- City: Rancho Cordova
- State: California
- Zip Code: 95742
- Country Name: United States
- Address: 11437 Sunrise Gold Cir Ste C, Rancho Cordova, California 95742, United States
- Country: United States

## Related Documents

- FDA Inspection 1210969 - Strings Restaurant Group - 2023-07-25 — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2023
- FDA Inspection 1210969 - Strings Restaurant Group - 2023-07-25 — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2023
- FDA Inspection 1052708 - Strings Restaurant Group - 2018-04-10 — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2018
- FDA Inspection 932196 - Strings Restaurant Group - 2015-05-21 — classification: No Action Indicated (NAI), source: FDA, date: May 21, 2015
- FDA Inspection 779230 - Strings Restaurant Group - 2012-04-27 — classification: No Action Indicated (NAI), source: FDA, date: April 27, 2012
- FDA Inspection 779230 - Strings Restaurant Group - 2012-04-27 — classification: No Action Indicated (NAI), source: FDA, date: April 27, 2012
- FDA Inspection 779230 - Strings Restaurant Group - 2012-04-27 — classification: No Action Indicated (NAI), source: FDA, date: April 27, 2012
- FDA Inspection 659169 - Strings Restaurant Group - 2010-04-28 — classification: No Action Indicated (NAI), source: FDA, date: April 28, 2010
- FDA Inspection 659169 - Strings Restaurant Group - 2010-04-28 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 28, 2010
- FDA Inspection 659169 - Strings Restaurant Group - 2010-04-28 — classification: No Action Indicated (NAI), source: FDA, date: April 28, 2010

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