FDA Inspection
Staubach Barror Water Systems Inc., DBA Aqua PureStaubach Barror Water Systems Inc., DBA Aqua Pure – FDA Inspection, Jan 8, 2016
Record Details
This FDA Inspection record concerns Staubach Barror Water Systems Inc., DBA Aqua Pure, with an inspection on January 8, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 8, 2016
- Product Type
- Devices
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ID · 921669b1-8974-4645-b463-3e24d99ca05f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 958070
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
6- 21 CFR 820.72(b)Calibration procedures - content
- 21 CFR 820.40Lack of procedures, or not maintained
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.22Quality Audit/Reaudit - conducted
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Other FDA inspections of Staubach Barror Water Systems Inc., DBA Aqua Pure
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 10, 2025 | NAI | Compliance: Devices | |
| January 31, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Staubach Barror Water Systems Inc., DBA Aqua Pure
- FDA Inspection 1296058 - 2025-12-10
- FDA Inspection 1196887 - 2023-01-31
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