# FDA Inspection 1263678 - Vayuclear Inc - March 14, 2025

Source: https://www.keypedia.com/records/fda_inspections/vayuclear-inc/9c01b898-bfd3-48a9-a9b4-e90cc539cde4
Source feed: FDA_Inspections

> FDA Inspection 1263678 for Vayuclear Inc on March 14, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1263678
- Company Name: Vayuclear Inc
- Inspection Date: 2025-03-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1263678 - 2025-03-14](https://www.keypedia.com/records/fda_inspections/vayuclear-inc/1a54eeba-fa16-4e49-8d00-060ef4768d81)
- [FDA Inspection 1263678 - 2025-03-14](https://www.keypedia.com/records/fda_inspections/vayuclear-inc/5330454e-d771-4d82-a0d4-08b01ad14550)
- [FDA Inspection 1263678 - 2025-03-14](https://www.keypedia.com/records/fda_inspections/vayuclear-inc/4441714c-2aa5-4459-b9a2-c0fd15235b1d)

Company: https://www.keypedia.com/companies/vayuclear-inc/86083840-ef4b-4ed8-a820-7e4fa5b05310

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