FDA Inspection
Phipps & Bird, Inc.Phipps & Bird, Inc. – FDA Inspection, Sep 18, 2012
Record Details
This FDA Inspection record concerns Phipps & Bird, Inc., with an inspection on September 18, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Phipps & Bird, Inc.
- Inspection Date
- September 18, 2012
- Product Type
- Devices
View Company Profile
ID · 0cd54507-5b22-486f-8706-1d359b703ec0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 799344
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.22Quality Audit/Reaudit - conducted
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Phipps & Bird, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 20, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 20, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Phipps & Bird, Inc.
- FDA Inspection 1069137 - 2018-09-20
- FDA Inspection 938993 - 2015-08-20
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