# FDA Inspection 1290048 - Zenflow, Inc. - October 30, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/zenflow-inc/2bc64dad-f9d6-4290-954b-00bdcf6c413e
Source feed: FDA_Inspections

> FDA Inspection 1290048 for Zenflow, Inc. on October 30, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1290048
- Company Name: Zenflow, Inc.
- Inspection Date: 2025-10-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: San Francisco District Office

## Related Documents

- [FDA Inspection 1273304 - 2025-06-06](https://www.globalkeysolutions.net/records/fda_inspections/zenflow-inc/c8a1acf6-8fa5-4074-aeae-f7f7f6a9e4e0)
- [FDA Inspection 1273304 - 2025-06-06](https://www.globalkeysolutions.net/records/fda_inspections/zenflow-inc/7044ac4a-74e3-4bd4-96dd-257ee915a346)

Company: https://www.globalkeysolutions.net/companies/zenflow-inc/8f15f8d4-6913-41a1-ad98-74860c35d1eb

Office: https://www.globalkeysolutions.net/offices/san-francisco-district-office/6f838e9c-aae1-4665-9c46-a51d43be02df