# Pasta-Bilities, Inc., Indianapolis, IN – FDA Inspections

Source: https://www.keypedia.com/companies/pasta-bilities-inc/87984d08-6134-42b7-8c81-c14efa352a42

> Inspection records and compliance data for Pasta-Bilities, Inc. in Indianapolis, Indiana. 6 FDA inspections on record, 1 Form 483, last inspected June 24, 2024.

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## Details

- Name: Pasta-Bilities, Inc.
- FEI Number: 3001236724
- Address Line 1: 6894 Hawthorn Park Dr
- City: Indianapolis
- State: Indiana
- Zip Code: 46220
- Country Name: United States
- Address: 6894 Hawthorn Park Dr, Indianapolis, Indiana 46220, United States
- Country: United States

## Related Documents

- [FDA Inspection 1242069 - Pasta-Bilities, Inc. - 2024-06-24](https://www.keypedia.com/records/fda_inspections/pasta-bilities-inc/4b529604-2231-4004-a9da-c4f2c480dabb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 24, 2024
- FDA Inspection 1242069 - Pasta-Bilities, Inc. - 2024-06-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 24, 2024
- FDA Inspection 1040127 - Pasta-Bilities, Inc. - 2018-02-06 — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2018
- [FDA Inspection 1040127 - Pasta-Bilities, Inc. - 2018-02-06](https://www.keypedia.com/records/fda_inspections/pasta-bilities-inc/a3bc22ea-c574-43f2-9b53-19b8446d7c41) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2018
- FDA Inspection 911470 - Pasta-Bilities, Inc. - 2015-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2015
- [FDA Inspection 756173 - Pasta-Bilities, Inc. - 2011-12-07](https://www.keypedia.com/records/fda_inspections/pasta-bilities-inc/dedbe2ed-b855-4043-a47d-62f611b28e5b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 7, 2011
- FDA Inspection 673008 - Pasta-Bilities, Inc. - 2010-07-08 — classification: No Action Indicated (NAI), source: FDA, date: July 8, 2010
- FDA Inspection 612347 - Pasta-Bilities, Inc. - 2009-09-10 — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2009

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