# FDA Inspection 1180871 - Gutizmultiservices Inc - September 29, 2022

Source: https://www.keypedia.com/records/fda_inspections/gutizmultiservices-inc/2b11fbc8-541a-4a5a-a899-7b03a4a127f4
Source feed: FDA_Inspections

> FDA Inspection 1180871 for Gutizmultiservices Inc on September 29, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180871
- Company Name: Gutizmultiservices Inc
- Inspection Date: 2022-09-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1180871 - 2022-09-29](https://www.keypedia.com/records/fda_inspections/gutizmultiservices-inc/95a3ae94-07a6-40b0-a099-abb38bb1492e)

Company: https://www.keypedia.com/companies/gutizmultiservices-inc/d077355e-99ca-4e03-af30-168c9df51ad1

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