# Probioferm, LLC, Urbandale, IA – FDA Inspections

Source: https://www.keypedia.com/companies/probioferm-llc/d9ee1ace-a62a-48bf-82ac-87c8d4bfc872

> Inspection records and compliance data for Probioferm, LLC in Urbandale, Iowa. 5 FDA inspections on record, 1 Form 483, last inspected February 22, 2023.

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## Details

- Name: Probioferm, LLC
- FEI Number: 3008515859
- Address Line 1: 10215 Dennis Dr
- City: Urbandale
- State: Iowa
- Zip Code: 50322
- Country Name: United States
- Address: 10215 Dennis Dr, Urbandale, Iowa 50322, United States
- Country: United States

## Related Documents

- FDA Inspection 1200077 - Probioferm, LLC - 2023-02-22 — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2023
- FDA Inspection 1200077 - Probioferm, LLC - 2023-02-22 — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2023
- FDA Inspection 1121906 - Probioferm, LLC - 2020-02-26 — classification: No Action Indicated (NAI), source: FDA, date: February 26, 2020
- FDA Inspection 1121906 - Probioferm, LLC - 2020-02-26 — classification: No Action Indicated (NAI), source: FDA, date: February 26, 2020
- [FDA Inspection 1010324 - Probioferm, LLC - 2017-01-27](https://www.keypedia.com/records/fda_inspections/probioferm-llc/f8aa2725-2cd3-476d-a936-11391f614ca2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 27, 2017
- FDA Inspection 1010324 - Probioferm, LLC - 2017-01-27 — classification: No Action Indicated (NAI), source: FDA, date: January 27, 2017
- FDA Inspection 885349 - Probioferm, LLC - 2014-06-26 — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2014
- FDA Inspection 885349 - Probioferm, LLC - 2014-06-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 26, 2014
- FDA Inspection 885349 - Probioferm, LLC - 2014-06-26 — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2014
- FDA Inspection 722529 - Probioferm, LLC - 2011-05-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 5, 2011

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