# Healthtex Distributors, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/healthtex-distributors-inc/f1b3a03e-f4d8-4dd0-b7e7-45295d95ea6b

> Inspection records and compliance data for Healthtex Distributors, Inc. in Miami, Florida. Access full analysis and detailed observations.

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## Details

- Name: Healthtex Distributors, Inc.
- FEI Number: 3000206696
- City: Miami
- State: Florida
- Country Name: United States
- Address Line 1: 3555 Nw 41st St
- Zip Code: 33142

## Related Documents

- [FDA Inspection 1224118 - Healthtex Distributors, Inc. - 2023-12-01](https://www.globalkeysolutions.net/records/fda_inspections/healthtex-distributors-inc/9288d3c9-9f5d-45c0-84e0-dd1bcdc25c73) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 1, 2023
- [WARNING_LETTER - Healthtex Distributors, Inc. - 2023-02-01](https://www.globalkeysolutions.net/records/warning_letter/healthtex-distributors-inc/9472ec42-1ee4-4b6d-b548-8f01813ef959) — source: FDA, date: February 1, 2023
- [FDA Inspection 1196648 - Healthtex Distributors, Inc. - 2023-02-01](https://www.globalkeysolutions.net/records/fda_inspections/healthtex-distributors-inc/7ce35e20-b4f0-48a1-99a4-12bb34b7ed5d) — classification: Official Action Indicated (OAI), source: FDA, date: February 1, 2023
- [FDA Inspection 1024503 - Healthtex Distributors, Inc. - 2017-09-01](https://www.globalkeysolutions.net/records/fda_inspections/healthtex-distributors-inc/027822ea-d4c6-45e4-a26d-ca2eb24746c2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 1, 2017
- [FDA Inspection 827602 - Healthtex Distributors, Inc. - 2013-04-17](https://www.globalkeysolutions.net/records/fda_inspections/healthtex-distributors-inc/83ee468f-93d6-4cfc-9a1d-629d48dd5f6f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 17, 2013
- [FDA Inspection 827602 - Healthtex Distributors, Inc. - 2013-04-17](https://www.globalkeysolutions.net/records/fda_inspections/healthtex-distributors-inc/0b4e069d-219e-40f1-8e15-0a493f6e7f7f) — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2013

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