# TENSproducts, LLC – FDA Inspection, Oct 31, 2011

Source: https://www.keypedia.com/records/fda_inspections/tensproducts-llc/9afc3d97-772d-4c73-90a9-cb54366712df
Source feed: FDA_Inspections

> FDA inspection 752304 of TENSproducts, LLC, October 31, 2011. Classification: Voluntary Action Indicated (VAI). 12 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 752304
- Company Name: TENSproducts, LLC
- Inspection Date: 2011-10-31
- 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: 12

## Related Documents

- FDA Inspection 1073144 - 2018-11-06
- FDA Inspection 909806 - 2014-10-01

Company: https://www.keypedia.com/companies/tensproducts-llc/d9d7d646-2bb1-46a4-87d6-cc2923659424

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