# Gourmet International Ltd. dba Niche Gourmet - Inspection Records

Source: https://www.globalkeysolutions.net/companies/gourmet-international-ltd-dba-niche-gourmet/645dc8c4-771b-419e-922c-b23b209a1b9c

> Inspection records and compliance data for Gourmet International Ltd. dba Niche Gourmet in Grand Rapids, Michigan. Access full analysis and detailed observations.

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## Details

- Name: Gourmet International Ltd. dba Niche Gourmet
- FEI Number: 1000139700
- City: Grand Rapids
- State: Michigan
- Country Name: United States
- Address Line 1: 5253 Patterson Ave Se
- Zip Code: 49512

## Related Documents

- [FDA Inspection 1200983 - Gourmet International Ltd. dba Niche Gourmet - 2023-03-27](https://www.globalkeysolutions.net/records/fda_inspections/gourmet-international-ltd-dba-niche-gourmet/967b16ae-56fa-43a4-95a0-49bcc0555677) — classification: No Action Indicated (NAI), source: FDA, date: March 27, 2023
- [FDA Inspection 1128546 - Gourmet International Ltd. dba Niche Gourmet - 2020-08-21](https://www.globalkeysolutions.net/records/fda_inspections/gourmet-international-ltd-dba-niche-gourmet/290e032a-c261-46df-985f-cc6083ffcf44) — classification: No Action Indicated (NAI), source: FDA, date: August 21, 2020
- [FDA Inspection 1110779 - Gourmet International Ltd. dba Niche Gourmet - 2019-11-14](https://www.globalkeysolutions.net/records/fda_inspections/gourmet-international-ltd-dba-niche-gourmet/3b74ed95-c5cf-4322-8ca9-dc35370b84fb) — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2019
- [FDA Inspection 1025692 - Gourmet International Ltd. dba Niche Gourmet - 2017-09-14](https://www.globalkeysolutions.net/records/fda_inspections/gourmet-international-ltd-dba-niche-gourmet/fc706d80-8853-4e2b-95d9-a34af2b0f36d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 14, 2017
- [FDA Inspection 926707 - Gourmet International Ltd. dba Niche Gourmet - 2015-05-18](https://www.globalkeysolutions.net/records/fda_inspections/gourmet-international-ltd-dba-niche-gourmet/a0930e03-aa52-430a-a6cb-058d48b0c79b) — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2015

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