# Hollywog LLC – FDA Inspection, Apr 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/hollywog-llc/40ed0485-b7de-4bb6-ace0-6ee82e3737cb
Source feed: FDA_Inspections

> FDA inspection 922023 of Hollywog LLC, April 17, 2015. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 922023
- Company Name: Hollywog LLC
- Inspection Date: 2015-04-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1326562 - 2026-07-16](https://www.keypedia.com/records/fda_inspections/hollywog-llc/18d0df3a-a1be-4490-9dad-258b66bd1baa)

Company: https://www.keypedia.com/companies/hollywog-llc/4e902eee-5ac2-40a3-8c8b-ea6c39696f52

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