# FDA Inspection 1110713 - Spectra Baby USA - November 22, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/spectra-baby-usa/4e3c3f42-0e5e-4aeb-a449-f1760bebbc4c
Source feed: FDA_Inspections

> FDA Inspection 1110713 for Spectra Baby USA on November 22, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1110713
- Company Name: Spectra Baby USA
- Inspection Date: 2019-11-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1110713 - 2019-11-22](https://www.globalkeysolutions.net/records/fda_inspections/spectra-baby-usa/ed0e2b77-db56-4797-a36a-9fe25d32becf)

Company: https://www.globalkeysolutions.net/companies/spectra-baby-usa/46dd95e7-c49b-44e0-a6eb-52d1894217e4

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