# FDA Inspection 1027028 - GeoTec, Inc. - September 29, 2017

Source: https://www.keypedia.com/records/fda_inspections/geotec-inc/bfcdc89d-666b-41b7-98b8-2a7bc7bbae86
Source feed: FDA_Inspections

> FDA Inspection 1027028 for GeoTec, Inc. on September 29, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1027028
- Company Name: GeoTec, Inc.
- Inspection Date: 2017-09-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/geotec-inc/1ad5a8c1-2917-44ce-913a-dbc93047ca01

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