# FDA Inspection 942206 - SOS Hyperlite Limited - August 12, 2015

Source: https://www.keypedia.com/records/fda_inspections/sos-hyperlite-limited/7d84c9b0-d84f-4432-8217-0ac05e0caab8
Source feed: FDA_Inspections

> FDA Inspection 942206 for SOS Hyperlite Limited on August 12, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 942206
- Company Name: SOS Hyperlite Limited
- Inspection Date: 2015-08-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/sos-hyperlite-limited/88d68e87-50d8-4148-9d8f-ff7b40d207b1

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