# Staubach Barror Water Systems Inc., DBA Aqua Pure – FDA Inspection, Jan 8, 2016

Source: https://www.keypedia.com/records/fda_inspections/staubach-barror-water-systems-inc-dba-aqua-pure/921669b1-8974-4645-b463-3e24d99ca05f
Source feed: FDA_Inspections

> FDA inspection 958070 of Staubach Barror Water Systems Inc., DBA Aqua Pure, January 08, 2016. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 958070
- Company Name: Staubach Barror Water Systems Inc., DBA Aqua Pure
- Inspection Date: 2016-01-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1296058 - 2025-12-10](https://www.keypedia.com/records/fda_inspections/staubach-barror-water-systems-inc-dba-aqua-pure/fda2f900-d5af-4ddc-8146-d74f417746a9)
- FDA Inspection 1196887 - 2023-01-31

Company: https://www.keypedia.com/companies/staubach-barror-water-systems-inc-dba-aqua-pure/34b5d8e8-6437-4a54-be4b-d6d2564c0e63

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7