# MICROVENTION INC. – FDA Inspection, Sep 25, 2015

Source: https://www.keypedia.com/records/fda_inspections/microvention-inc/6819729d-39be-4b86-a4a6-aca1c2764a34
Source feed: FDA_Inspections

> FDA inspection 943775 of MICROVENTION INC., September 25, 2015. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 943775
- Company Name: MICROVENTION INC.
- Inspection Date: 2015-09-25
- 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: 1

## Related Documents

- [FDA Inspection 1205080 - 2023-05-04](https://www.keypedia.com/records/fda_inspections/microvention-inc/a5d5a852-a6a1-4e5d-b32d-19f7d0a08888)
- FDA Inspection 1155400 - 2021-06-22
- FDA Inspection 1077480 - 2019-01-17
- FDA Inspection 1074141 - 2018-11-29
- FDA Inspection 757144 - 2011-12-13

Company: https://www.keypedia.com/companies/microvention-inc/b921bdf2-a18a-474f-9dfd-0fd35ed60dac

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