# FDA Inspection 987200 - Pelican Biothermal - March 31, 2016

Source: https://www.keypedia.com/records/fda_inspections/pelican-biothermal/1a15ec47-ea46-4f27-bcfe-8f3902f7bfc7
Source feed: FDA_Inspections

> FDA Inspection 987200 for Pelican Biothermal on March 31, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987200
- Company Name: Pelican Biothermal
- Inspection Date: 2016-03-31
- 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/pelican-biothermal/ca5c687a-77c5-489a-a2bb-d74f696f1a63

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