FDA Inspection
Progressive Surgical ProductsProgressive Surgical Products – FDA Inspection, Jun 25, 2012
Record Details
This FDA Inspection record concerns Progressive Surgical Products, with an inspection on June 25, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 25, 2012
- Product Type
- Devices
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ID · 46dbfbd9-d3f5-4bca-acc9-1b2144480e5a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 788107
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.100(b)Documentation
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 803.17(a)(3)Lack of System for Timely Submission of Reports
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Other FDA inspections of Progressive Surgical Products
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 18, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Progressive Surgical Products
- FDA Inspection 629642 - 2009-11-18
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