FDA Inspection
PT Products, LLCPT Products, LLC – FDA Inspection, May 20, 2009
Record Details
This FDA Inspection record concerns PT Products, LLC, with an inspection on May 20, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- PT Products, LLC
- Inspection Date
- May 20, 2009
- Product Type
- Devices
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ID · 3d1c473e-aa10-47a7-8cef-3155495c0bc1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 579699
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.80(e)Documentation
- 21 CFR 820.198(a)General
- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of PT Products, LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 27, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for PT Products, LLC
- FDA Inspection 838131 - 2013-06-27
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