# LightScalpel, Inc. – FDA Inspection, Jun 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/lightscalpel-inc/b99113f1-e995-4f37-a2c1-6406091432b7
Source feed: FDA_Inspections

> FDA inspection 976441 of LightScalpel, Inc., June 29, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 976441
- Company Name: LightScalpel, Inc.
- Inspection Date: 2016-06-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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- [FDA Inspection 868843 - 2014-02-27](https://www.keypedia.com/records/fda_inspections/lightscalpel-inc/7c6e7b6e-07d1-4d11-a9cc-e96e9ade15f8)
- FDA Inspection 765194 - 2012-01-24

Company: https://www.keypedia.com/companies/lightscalpel-inc/f91f6b0d-bad8-4578-9dcc-d4fb4191a6be

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