# FDA Inspection 940208 - UniStrip Technologies, LLC - August 19, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/unistrip-technologies-llc/dc030d15-28d8-4a0a-abec-ec9ff1d32a16
Source feed: FDA_Inspections

> FDA Inspection 940208 for UniStrip Technologies, LLC on August 19, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 940208
- Company Name: UniStrip Technologies, LLC
- Inspection Date: 2015-08-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1098811 - 2019-05-01](https://www.globalkeysolutions.net/records/fda_inspections/unistrip-technologies-llc/d27f4b5f-ad56-4569-b19e-19ec38633a87)
- [FDA Inspection 1098811 - 2019-05-01](https://www.globalkeysolutions.net/records/fda_inspections/unistrip-technologies-llc/1278c554-9f06-4013-87ae-e4dc3b161515)
- [FDA Inspection 940208 - 2015-08-19](https://www.globalkeysolutions.net/records/fda_inspections/unistrip-technologies-llc/9d4e6280-6cd6-4274-a5fc-9b6ffb1121d2)

Company: https://www.globalkeysolutions.net/companies/unistrip-technologies-llc/87058ac2-8bfd-4794-8eb6-7cb141b99d51

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