# H. Brooks & Company, LLC - Inspection Records

Source: https://www.keypedia.com/companies/h-brooks-company-llc/e2a1c488-c08f-4f2e-abd8-e4ffc0a607b2

> Inspection records and compliance data for H. Brooks & Company, LLC in New Brighton, Minnesota. 8 FDA inspections on record, last inspected July 24, 2019.

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## Details

- Name: H. Brooks & Company, LLC
- FEI Number: 3003315236
- Address Line 1: 600 Lakeview Point Dr
- City: New Brighton
- State: Minnesota
- Zip Code: 55112
- Country Name: United States
- Address: 600 Lakeview Point Dr, New Brighton, Minnesota 55112, United States
- Country: United States

## Related Documents

- [483 - H. Brooks & Company, LLC - 2019-07-24](https://www.keypedia.com/records/483/h-brooks-company-llc/34d0deef-764a-4a84-b926-5f2d367ed11e) — source: FDA, date: July 24, 2019
- [FDA Inspection 1097327 - H. Brooks & Company, LLC - 2019-07-24](https://www.keypedia.com/records/fda_inspections/h-brooks-company-llc/7ce2d1ac-8c9e-4ffc-830a-c65f2feb8268) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 24, 2019
- FDA Inspection 900654 - H. Brooks & Company, LLC - 2014-10-23 — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2014
- FDA Inspection 782921 - H. Brooks & Company, LLC - 2012-05-23 — classification: No Action Indicated (NAI), source: FDA, date: May 23, 2012
- FDA Inspection 677557 - H. Brooks & Company, LLC - 2010-08-26 — classification: No Action Indicated (NAI), source: FDA, date: August 26, 2010
- FDA Inspection 587048 - H. Brooks & Company, LLC - 2009-06-08 — classification: No Action Indicated (NAI), source: FDA, date: June 8, 2009
- FDA Inspection 554846 - H. Brooks & Company, LLC - 2009-01-07 — classification: No Action Indicated (NAI), source: FDA, date: January 7, 2009
- FDA Inspection 547970 - H. Brooks & Company, LLC - 2008-11-12 — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2008
- FDA Inspection 547965 - H. Brooks & Company, LLC - 2008-11-12 — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2008

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