# Medaus, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/medaus-inc/19fae749-cee3-4578-a7b4-46baab199483

> Inspection records and compliance data for Medaus, Inc. in Hoover, Alabama. Access full analysis and detailed observations.

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## Details

- Name: Medaus, Inc.
- FEI Number: 3001298034
- City: Hoover
- State: Alabama
- Country Name: United States
- Address Line 1: 6801 Cahaba Valley Rd Ste 116
- Zip Code: 35242
- Facility Type: Producer of Sterile Products

## Related Documents

- [483 - Medaus, Inc. - 2016-03-11](https://www.keypedia.com/records/483/medaus-inc/54ba35de-f831-48de-a230-d6012c09150c) — source: FDA, date: March 11, 2016
- [WARNING_LETTER - Medaus, Inc. - 2016-03-11](https://www.keypedia.com/records/warning_letter/medaus-inc/51d84724-5468-4777-a9db-64f0b7e02c11) — source: FDA, date: March 11, 2016
- [FDA Inspection 964477 - Medaus, Inc. - 2016-03-11](https://www.keypedia.com/records/fda_inspections/medaus-inc/7937f6b5-df91-47de-bf92-4c17381cfc71) — classification: Official Action Indicated (OAI), source: FDA, date: March 11, 2016
- [FDA_REQUESTED_RECALL_LETTER - Medaus, Inc. - 2016-03-09](https://www.keypedia.com/records/fda_requested_recall_letter/medaus-inc/97ab66cd-bfed-4b62-b7ce-c3be72495dde) — source: FDA, date: March 9, 2016
- [WARNING_LETTER - Medaus, Inc. - 2013-03-22](https://www.keypedia.com/records/warning_letter/medaus-inc/31073110-5bfd-4cc7-a678-1710a8b75858) — source: FDA, date: March 22, 2013
- [483 - Medaus, Inc. - 2013-03-22](https://www.keypedia.com/records/483/medaus-inc/f328372c-14d6-42dc-bc78-a6b3235c161d) — source: FDA, date: March 22, 2013
- [FDA Inspection 824093 - Medaus, Inc. - 2013-03-22](https://www.keypedia.com/records/fda_inspections/medaus-inc/9a54abed-4d8c-4ce0-affe-40b6810f8951) — classification: Official Action Indicated (OAI), source: FDA, date: March 22, 2013
- [FDA Inspection 571229 - Medaus, Inc. - 2009-02-12](https://www.keypedia.com/records/fda_inspections/medaus-inc/e0e0e7a4-70a5-4413-9b2b-331131fff1d5) — classification: Official Action Indicated (OAI), source: FDA, date: February 12, 2009

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