# FDA Inspection 986018 - Surgik LC - September 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/surgik-lc/eb7ce943-3fb1-4c14-a9cd-ccca8fb89f43
Source feed: FDA_Inspections

> FDA Inspection 986018 for Surgik LC on September 16, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 986018
- Company Name: Surgik LC
- Inspection Date: 2016-09-16
- 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 986018 - 2016-09-16](https://www.keypedia.com/records/fda_inspections/surgik-lc/15b16bdb-c225-432d-842a-fbcf7bbf9c7d)

Company: https://www.keypedia.com/companies/surgik-lc/45a07ada-4146-4100-ad07-a673f374e8e9

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