# FDA Inspection 960125 - Purple Surgical Manufacturing Limited - February 04, 2016

Source: https://www.keypedia.com/records/fda_inspections/purple-surgical-manufacturing-limited/3e79bb36-d3a6-40fe-b7c2-efebdb907351
Source feed: FDA_Inspections

> FDA Inspection 960125 for Purple Surgical Manufacturing Limited on February 04, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960125
- Company Name: Purple Surgical Manufacturing Limited
- Inspection Date: 2016-02-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 960125 - 2016-02-04](https://www.keypedia.com/records/fda_inspections/purple-surgical-manufacturing-limited/befe8f11-75b0-4b64-a4f7-094c1e542e0d)

Company: https://www.keypedia.com/companies/purple-surgical-manufacturing-limited/09594708-d758-49e3-a654-e234ccd966cf

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