# Garden Cut, LLC, Indianapolis, IN – FDA Inspections

Source: https://www.keypedia.com/companies/garden-cut-llc/541b23c4-1a92-47bd-af28-778b32beca78

> Inspection records and compliance data for Garden Cut, LLC in Indianapolis, Indiana. 6 FDA inspections on record, 2 Form 483s, last inspected January 29, 2025.

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## Details

- Name: Garden Cut, LLC
- FEI Number: 3010634784
- Address Line 1: 4501 Massachusetts Ave
- City: Indianapolis
- State: Indiana
- Zip Code: 46218
- Country Name: United States
- Address: 4501 Massachusetts Ave, Indianapolis, Indiana 46218, United States
- Country: United States

## Related Documents

- FDA Inspection 1261731 - Garden Cut, LLC - 2025-01-29 — source: FDA, date: January 29, 2025
- FDA Inspection 1261731 - Garden Cut, LLC - 2025-01-29 — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2025
- FDA Inspection 1261731 - Garden Cut, LLC - 2025-01-29 — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2025
- FDA Inspection 1245758 - Garden Cut, LLC - 2024-08-07 — source: FDA, date: August 7, 2024
- FDA Inspection 1152988 - Garden Cut, LLC - 2021-09-17 — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2021
- FDA Inspection 1152988 - Garden Cut, LLC - 2021-09-17 — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2021
- [FDA Inspection 1065451 - Garden Cut, LLC - 2018-09-13](https://www.keypedia.com/records/fda_inspections/garden-cut-llc/ed5b5827-1fc7-476a-9325-850eb4af908d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 13, 2018
- FDA Inspection 1065451 - Garden Cut, LLC - 2018-09-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 13, 2018
- [FDA Inspection 1024015 - Garden Cut, LLC - 2017-09-01](https://www.keypedia.com/records/fda_inspections/garden-cut-llc/02f7dd9c-ea7a-47ea-a4b3-18fa79a203fa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 1, 2017
- FDA Inspection 985818 - Garden Cut, LLC - 2016-07-20 — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2016

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