# Hollywog LLC – FDA Inspection, Jul 16, 2026

Source: https://www.keypedia.com/records/fda_inspections/hollywog-llc/18d0df3a-a1be-4490-9dad-258b66bd1baa
Source feed: FDA_Inspections

> FDA inspection 1326562 of Hollywog LLC, July 16, 2026. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1326562
- Company Name: Hollywog LLC
- Inspection Date: 2026-07-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New Orleans District Office
- Citation Count: 1

## Related Documents

- [FDA Inspection 922023 - 2015-04-17](https://www.keypedia.com/records/fda_inspections/hollywog-llc/40ed0485-b7de-4bb6-ace0-6ee82e3737cb)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/nikki-s-bryant/fe859d4f-23a6-4bc9-94c6-5b3c3fe8d99a)

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

Office: https://www.keypedia.com/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea