# FDA Inspection 1100132 - Bloomlife Inc. - August 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/bloomlife-inc/12a748b8-01a8-4eb7-8127-04e5554cdcd7
Source feed: FDA_Inspections

> FDA Inspection 1100132 for Bloomlife Inc. on August 07, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100132
- Company Name: Bloomlife Inc.
- Inspection Date: 2019-08-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/bloomlife-inc/d02682f6-a2a1-4ac1-92dc-60440b2916d9

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