# Lushlife Gardens - Inspection Records

Source: https://www.keypedia.com/companies/lushlife-gardens/9b161c0a-d027-4715-bec7-2fe14de226fc

> Inspection records and compliance data for Lushlife Gardens in Milford, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Lushlife Gardens
- FEI Number: 3003056121
- City: Milford
- State: New Jersey
- Country Name: United States
- Address Line 1: 202 Mount Nebo Rd, P.O. Box 554
- Zip Code: 08848

## Related Documents

- [FDA Inspection 922779 - Lushlife Gardens - 2015-04-16](https://www.keypedia.com/records/fda_inspections/lushlife-gardens/cc2a2016-5d6f-4300-80d0-8205e8156eed) — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2015
- [FDA Inspection 869801 - Lushlife Gardens - 2014-03-10](https://www.keypedia.com/records/fda_inspections/lushlife-gardens/8b8de43b-7350-4b08-87cd-5752cfb5290f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 10, 2014
- [FDA Inspection 806306 - Lushlife Gardens - 2012-10-15](https://www.keypedia.com/records/fda_inspections/lushlife-gardens/570091b8-a0b2-41be-b763-c5203aa72dd7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2012
- [FDA Inspection 768541 - Lushlife Gardens - 2012-02-09](https://www.keypedia.com/records/fda_inspections/lushlife-gardens/fa861c1a-2b90-4a3d-8833-70899d1a4932) — classification: Official Action Indicated (OAI), source: FDA, date: February 9, 2012
- [WARNING_LETTER - Lushlife Gardens - 2011-11-21](https://www.keypedia.com/records/warning_letter/lushlife-gardens/2cccc195-36c0-4ccc-b0e1-2aee3b195537) — source: FDA, date: November 21, 2011
- [FDA Inspection 754454 - Lushlife Gardens - 2011-11-21](https://www.keypedia.com/records/fda_inspections/lushlife-gardens/f5d4a3d6-3785-4c83-a90f-a817dd6a5b23) — classification: Official Action Indicated (OAI), source: FDA, date: November 21, 2011
- [FDA Inspection 586239 - Lushlife Gardens - 2009-06-01](https://www.keypedia.com/records/fda_inspections/lushlife-gardens/44607b42-56ec-42c6-b879-1b4eb2629af2) — classification: No Action Indicated (NAI), source: FDA, date: June 1, 2009

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