# Helena Laboratories, Corp., Beaumont, TX – FDA Inspections

Source: https://www.keypedia.com/companies/helena-laboratories-corp/9742bc61-dee7-4b93-a33a-0581bd422d44

> Inspection records and compliance data for Helena Laboratories, Corp. in Beaumont, Texas. 4 FDA inspections on record (1 OAI), 2 Form 483s, last inspected December 14, 2018.

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## Details

- Name: Helena Laboratories, Corp.
- FEI Number: 1618982
- Address Line 1: 1530 Lindbergh Dr
- City: Beaumont
- State: Texas
- Zip Code: 77707
- Country Name: United States
- Address: 1530 Lindbergh Dr, Beaumont, Texas 77707, United States
- Country: United States

## Related Documents

- FDA Inspection 1074463 - Helena Laboratories, Corp. - 2018-12-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 14, 2018
- [FDA Inspection 1074463 - Helena Laboratories, Corp. - 2018-12-14](https://www.keypedia.com/records/fda_inspections/helena-laboratories-corp/cb1d01a8-02e8-4222-96c5-3ece78757b47) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 14, 2018
- FDA Inspection 1018711 - Helena Laboratories, Corp. - 2017-07-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2017
- [FDA Inspection 1018711 - Helena Laboratories, Corp. - 2017-07-21](https://www.keypedia.com/records/fda_inspections/helena-laboratories-corp/86bce6a3-dd81-4f06-8a99-8f01698ec8ea) — classification: Official Action Indicated (OAI), source: FDA, date: July 21, 2017
- [FDA Inspection 820597 - Helena Laboratories, Corp. - 2013-03-01](https://www.keypedia.com/records/fda_inspections/helena-laboratories-corp/92e8404f-4bfd-4aba-8b2d-bf38577293de) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2013
- FDA Inspection 820597 - Helena Laboratories, Corp. - 2013-03-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2013
- FDA Inspection 694963 - Helena Laboratories, Corp. - 2010-10-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 29, 2010
- FDA Inspection 694963 - Helena Laboratories, Corp. - 2010-10-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 29, 2010

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