# Biometerplususa Inc. – FDA Inspection, Jul 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/biometerplususa-inc/3c99db4a-3e9e-4680-bbde-5e76cda282a1
Source feed: FDA_Inspections

> FDA inspection 981334 of Biometerplususa Inc., July 21, 2016. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 981334
- Company Name: Biometerplususa Inc.
- Inspection Date: 2016-07-21
- 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 1309260 - 2026-03-25](https://www.keypedia.com/records/fda_inspections/biometerplususa-inc/376d11e3-af1a-4aac-90b5-f1e4105c62c3)
- FDA Inspection 722592 - 2011-05-03
- [FDA Inspection 658684 - 2010-05-14](https://www.keypedia.com/records/fda_inspections/biometerplususa-inc/a3152694-bc43-465e-ac6b-5ada40dc3e16)
- FDA Inspection 615040 - 2009-09-25

Company: https://www.keypedia.com/companies/biometerplususa-inc/40694a01-d248-44ff-805c-763bbd5cb204

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