# Pulses America, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/pulses-america-inc/c2dc224b-40ec-4e46-accc-22b51775c077

> Inspection records and compliance data for Pulses America, Inc. in Northwood, North Dakota. Access full analysis and detailed observations.

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## Details

- Name: Pulses America, Inc.
- FEI Number: 3004334008
- City: Northwood
- State: North Dakota
- Country Name: United States
- Address Line 1: 301 S Potato Rd
- Zip Code: 58267

## Related Documents

- [FDA Inspection 1156757 - Pulses America, Inc. - 2021-11-15](https://www.globalkeysolutions.net/records/fda_inspections/pulses-america-inc/51548019-52e1-4ce7-8675-851f05356aff) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 15, 2021
- [FDA Inspection 1028249 - Pulses America, Inc. - 2017-10-06](https://www.globalkeysolutions.net/records/fda_inspections/pulses-america-inc/5e54ba44-4284-472d-9a87-09db2be87227) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 6, 2017
- [FDA Inspection 907527 - Pulses America, Inc. - 2014-12-05](https://www.globalkeysolutions.net/records/fda_inspections/pulses-america-inc/68626233-f110-4e21-b465-585521890a75) — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2014
- [FDA Inspection 782794 - Pulses America, Inc. - 2012-04-18](https://www.globalkeysolutions.net/records/fda_inspections/pulses-america-inc/8a2198c5-195b-4371-afd7-341bf67f9045) — classification: No Action Indicated (NAI), source: FDA, date: April 18, 2012
- [FDA Inspection 668347 - Pulses America, Inc. - 2010-06-25](https://www.globalkeysolutions.net/records/fda_inspections/pulses-america-inc/482b573d-cc54-412f-875c-99bc6eb1d1c7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 25, 2010
- [FDA Inspection 631002 - Pulses America, Inc. - 2009-11-24](https://www.globalkeysolutions.net/records/fda_inspections/pulses-america-inc/c9d8c2b1-34a4-4aa0-bcca-ac7533b44c06) — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2009

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