# Munchkin Inc – FDA Inspection, Jan 19, 2018

Source: https://www.keypedia.com/records/fda_inspections/munchkin-inc/f7507b68-664e-4487-ae1e-70b06c2adace
Source feed: FDA_Inspections

> FDA inspection 1038408 of Munchkin Inc, January 19, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038408
- Company Name: Munchkin Inc
- Inspection Date: 2018-01-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1155216 - 2021-10-07](https://www.keypedia.com/records/fda_inspections/munchkin-inc/6d93fc5d-f8bf-4743-b3ab-bf7706564b52)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

Company: https://www.keypedia.com/companies/munchkin-inc/c388c623-f141-466f-9287-f57fe263450c

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