# Conformis, Inc. – FDA Inspection, Sep 20, 2019

Source: https://www.keypedia.com/records/fda_inspections/conformis-inc/c5f9d5ba-6057-4920-8de1-4214b9d89420
Source feed: FDA_Inspections

> FDA inspection 1102363 of Conformis, Inc., September 20, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102363
- Company Name: Conformis, Inc.
- Inspection Date: 2019-09-20
- 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: 2

## Related Documents

- [FDA Inspection 1199287 - 2023-03-09](https://www.keypedia.com/records/fda_inspections/conformis-inc/b31dd215-8ab1-45b9-87b9-0c4643a84748)
- [FDA Inspection 1064815 - 2018-09-07](https://www.keypedia.com/records/fda_inspections/conformis-inc/e8edafe7-8085-46b1-8f7e-b96260c6f0e3)
- FDA Inspection 929855 - 2015-06-12
- FDA Inspection 823060 - 2013-03-18

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gregson-a-joseph/90bf8118-3f32-4f44-95c4-fcde1f741a18)

Company: https://www.keypedia.com/companies/conformis-inc/4d049221-15de-4b53-addf-68ea7fed8cbc

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