# LCD Enterprises I, LLC d.b.a. The Sandwich Man - Inspection Records

Source: https://www.keypedia.com/companies/lcd-enterprises-i-llc-dba-the-sandwich-man/b64f4416-d373-423f-a9d1-593039d8583a

> Inspection records and compliance data for LCD Enterprises I, LLC d.b.a. The Sandwich Man in Pearl River, Louisiana. Access full analysis and detailed observations.

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## Details

- Name: LCD Enterprises I, LLC d.b.a. The Sandwich Man
- FEI Number: 2312303
- City: Pearl River
- State: Louisiana
- Country Name: United States
- Address Line 1: 65275 Highway 41
- Zip Code: 70452

## Related Documents

- [FDA Inspection 1027130 - LCD Enterprises I, LLC d.b.a. The Sandwich Man - 2017-05-26](https://www.keypedia.com/records/fda_inspections/lcd-enterprises-i-llc-dba-the-sandwich-man/8ab81cf6-925e-4b42-80cb-4b759669fe2e) — classification: No Action Indicated (NAI), source: FDA, date: May 26, 2017
- [FDA Inspection 921880 - LCD Enterprises I, LLC d.b.a. The Sandwich Man - 2015-04-10](https://www.keypedia.com/records/fda_inspections/lcd-enterprises-i-llc-dba-the-sandwich-man/e9ea5ec0-579a-4602-a555-02f3245cbe89) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2015
- [FDA Inspection 777118 - LCD Enterprises I, LLC d.b.a. The Sandwich Man - 2012-04-13](https://www.keypedia.com/records/fda_inspections/lcd-enterprises-i-llc-dba-the-sandwich-man/192611cd-d630-4ea3-ac85-1bf6a68ada3a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 13, 2012
- [FDA Inspection 725244 - LCD Enterprises I, LLC d.b.a. The Sandwich Man - 2011-05-19](https://www.keypedia.com/records/fda_inspections/lcd-enterprises-i-llc-dba-the-sandwich-man/cf0d9a0e-c811-48ff-b859-77529e39ceb9) — classification: Official Action Indicated (OAI), source: FDA, date: May 19, 2011
- [FDA Inspection 672540 - LCD Enterprises I, LLC d.b.a. The Sandwich Man - 2010-07-21](https://www.keypedia.com/records/fda_inspections/lcd-enterprises-i-llc-dba-the-sandwich-man/d663869c-72c9-4a86-b88a-db5dae961359) — classification: Official Action Indicated (OAI), source: FDA, date: July 21, 2010

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