# Huvepharma, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/huvepharma-inc/f7e97afe-1efa-4ded-a347-4bbed4c74058

> Inspection records and compliance data for Huvepharma, Inc. in Longmont, Colorado. Access full analysis and detailed observations.

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## Details

- Name: Huvepharma, Inc.
- FEI Number: 1910641
- City: Longmont
- State: Colorado
- Country Name: United States
- Address Line 1: 1301 Iowa Ave
- Zip Code: 80501

## Related Documents

- [483 - Huvepharma, Inc. - 2019-04-23](https://www.keypedia.com/records/483/huvepharma-inc/859eb647-fc77-465f-ba36-9c4c025f4384) — source: FDA, date: April 23, 2019
- [FDA Inspection 1087819 - Huvepharma, Inc. - 2019-04-23](https://www.keypedia.com/records/fda_inspections/huvepharma-inc/53019d59-7c8e-48ec-9eaf-15e782c993c5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 23, 2019
- [FDA Inspection 1018414 - Huvepharma, Inc. - 2017-07-14](https://www.keypedia.com/records/fda_inspections/huvepharma-inc/47b6cc03-5c74-4099-a349-d69a357e49e8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 14, 2017
- [FDA Inspection 952502 - Huvepharma, Inc. - 2015-12-04](https://www.keypedia.com/records/fda_inspections/huvepharma-inc/99168f48-6a59-459d-b5c2-a2f150f77ed4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 4, 2015
- [FDA Inspection 859555 - Huvepharma, Inc. - 2013-12-12](https://www.keypedia.com/records/fda_inspections/huvepharma-inc/ca4f2879-4d66-4291-a09c-f54e58944e31) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 12, 2013
- [FDA Inspection 769005 - Huvepharma, Inc. - 2012-02-21](https://www.keypedia.com/records/fda_inspections/huvepharma-inc/1008f632-af3d-4a73-813f-d60b91938ce2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 21, 2012
- [FDA Inspection 669707 - Huvepharma, Inc. - 2010-06-09](https://www.keypedia.com/records/fda_inspections/huvepharma-inc/a92f618d-2e3d-49e4-aea9-ce143773e8cf) — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010

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