# Tenacore LLC – FDA Inspection, Aug 22, 2018

Source: https://www.keypedia.com/records/fda_inspections/tenacore-llc/6a2f5936-0709-4e28-9c05-87562c55c881
Source feed: FDA_Inspections

> FDA inspection 1066010 of Tenacore LLC, August 22, 2018. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066010
- Company Name: Tenacore LLC
- Inspection Date: 2018-08-22
- 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: 1

## Related Documents

- [FDA Inspection 1328304 - 2026-07-24](https://www.keypedia.com/records/fda_inspections/tenacore-llc/151b522d-023a-4743-b312-081332a76a60)

## Related Officers

- [Wilfred A. Darang](https://www.keypedia.com/people/wilfred-a-darang/f0f1e653-891d-47d6-82e3-5ce40a5d3635)

Company: https://www.keypedia.com/companies/tenacore-llc/588d7f5f-4ca1-4789-8f5d-77e67d6cf6d1

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