FDA Inspection
Precision Systems, Inc.Precision Systems, Inc. – FDA Inspection, May 5, 2011
Record Details
This FDA Inspection record concerns Precision Systems, Inc., with an inspection on May 5, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Precision Systems, Inc.
- Inspection Date
- May 5, 2011
- Product Type
- Devices
View Company Profile
ID · 451c422f-7699-4b3a-9ece-4698c38adff9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 725010
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
6- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product control
- 21 CFR 820.184DHR content
- 21 CFR 820.20(b)Lack of or inadequate organizational structure
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Other FDA inspections of Precision Systems, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 14, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 23, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Precision Systems, Inc.
- FDA Inspection 1100229 - 2019-08-14
- FDA Inspection 833531 - 2013-05-23
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