# FDA Inspection 1032115 - Bolder Surgical, LLC - November 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/bolder-surgical-llc/a05cd0bb-bdef-49c4-ba44-343573481c78
Source feed: FDA_Inspections

> FDA Inspection 1032115 for Bolder Surgical, LLC on November 27, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032115
- Company Name: Bolder Surgical, LLC
- Inspection Date: 2017-11-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/bolder-surgical-llc/ebf174ab-a846-429d-b573-ea18c0e9b772

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