# Invivoscribe Technologies, Inc. – FDA Inspection, Mar 6, 2017

Source: https://www.keypedia.com/records/fda_inspections/invivoscribe-technologies-inc/f7a4ebdc-e397-43d7-85cc-ad14c07c912f
Source feed: FDA_Inspections

> FDA inspection 1006006 of Invivoscribe Technologies, Inc., March 06, 2017. Classification: No Action Indicated (NAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1006006
- Company Name: Invivoscribe Technologies, Inc.
- Inspection Date: 2017-03-06
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1248327 - 2024-08-14
- FDA Inspection 1072296 - 2018-11-01
- FDA Inspection 1001718 - 2017-02-06
- [FDA Inspection 898383 - 2014-09-17](https://www.keypedia.com/records/fda_inspections/invivoscribe-technologies-inc/5cfd25ac-0dc3-4789-986e-f00f4c9e33e4)

## Related Officers

- Issuing Officer
- [Issuing Officer](https://www.keypedia.com/people/scott-k-zika/7f967edd-5151-438b-a0e7-dd1db8a227d1)
- [Theresa Kirkham](https://www.keypedia.com/people/theresa-kirkham/c7d8aad0-d162-4fac-a1ba-4649c36fd714)

Company: https://www.keypedia.com/companies/invivoscribe-technologies-inc/d259e529-ccfc-4ba4-a18d-dea58e100ed9

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