# Microvention, Inc. – FDA Inspection, Aug 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/microvention-inc/949bee0e-b5c6-420d-85a9-f6a2085cae31
Source feed: FDA_Inspections

> FDA inspection 986764 of Microvention, Inc., August 25, 2016. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 986764
- Company Name: Microvention, Inc.
- Inspection Date: 2016-08-25
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1258987 - 2025-01-08
- FDA Inspection 1153926 - 2021-05-24
- [FDA Inspection 915040 - 2015-01-28](https://www.keypedia.com/records/fda_inspections/microvention-inc/c13f7fad-5f17-4546-8b2a-7b935817a6f7)
- FDA Inspection 830029 - 2013-04-30
- FDA Inspection 629675 - 2009-11-20

Company: https://www.keypedia.com/companies/microvention-inc/6f33f8be-5989-4888-ae8e-06cc18aa9242

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