# Miracapo Pizza Company, LLC dba Little Lady Foods Inc, Elk Grove Village, IL – FDA Inspections

Source: https://www.keypedia.com/companies/miracapo-pizza-company-llc-dba-little-lady-foods-inc/48a288ad-524e-4757-b422-fadfd842e961

> Inspection records and compliance data for Miracapo Pizza Company, LLC dba Little Lady Foods Inc in Elk Grove Village, Illinois. 5 FDA inspections on record, last inspected July 14, 2023.

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## Details

- Name: Miracapo Pizza Company, LLC dba Little Lady Foods Inc
- FEI Number: 1000115226
- Address Line 1: 2323 Pratt Blvd
- City: Elk Grove Village
- State: Illinois
- Zip Code: 60007
- Country Name: United States
- Address: 2323 Pratt Blvd, Elk Grove Village, Illinois 60007, United States
- Country: United States

## Related Documents

- FDA Inspection 1210714 - Miracapo Pizza Company, LLC dba Little Lady Foods Inc - 2023-07-14 — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2023
- FDA Inspection 1210714 - Miracapo Pizza Company, LLC dba Little Lady Foods Inc - 2023-07-14 — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2023
- FDA Inspection 1114515 - Miracapo Pizza Company, LLC dba Little Lady Foods Inc - 2019-10-11 — classification: No Action Indicated (NAI), source: FDA, date: October 11, 2019
- FDA Inspection 1114515 - Miracapo Pizza Company, LLC dba Little Lady Foods Inc - 2019-10-11 — classification: No Action Indicated (NAI), source: FDA, date: October 11, 2019
- [FDA Inspection 977030 - Miracapo Pizza Company, LLC dba Little Lady Foods Inc - 2016-05-06](https://www.keypedia.com/records/fda_inspections/miracapo-pizza-company-llc-dba-little-lady-foods-inc/be99d188-0a25-4453-8698-794b5a45531c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 6, 2016
- FDA Inspection 807738 - Miracapo Pizza Company, LLC dba Little Lady Foods Inc - 2012-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2012
- FDA Inspection 586502 - Miracapo Pizza Company, LLC dba Little Lady Foods Inc - 2009-06-04 — classification: No Action Indicated (NAI), source: FDA, date: June 4, 2009

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