# FDA Inspection 629642 - Progressive Surgical Products - November 18, 2009

Source: https://www.keypedia.com/records/fda_inspections/progressive-surgical-products/443dffc3-a407-4472-8b01-0781ea5e72a2
Source feed: FDA_Inspections

> FDA Inspection 629642 for Progressive Surgical Products on November 18, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 629642
- Company Name: Progressive Surgical Products
- Inspection Date: 2009-11-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 788107 - 2012-06-25](https://www.keypedia.com/records/fda_inspections/progressive-surgical-products/46dbfbd9-d3f5-4bca-acc9-1b2144480e5a)
- [FDA Inspection 629642 - 2009-11-18](https://www.keypedia.com/records/fda_inspections/progressive-surgical-products/ec6e22cf-b986-486a-bcb5-8c951f8c646b)

Company: https://www.keypedia.com/companies/progressive-surgical-products/cc6d0682-58e3-48e7-9248-d9b9d7ccee3a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7