# Dermazone LLC, Saint Petersburg, FL – FDA Inspections

Source: https://www.keypedia.com/companies/dermazone-llc/f871f692-cada-4e9c-bc1f-653b6f849434

> Inspection records and compliance data for Dermazone LLC in Saint Petersburg, Florida. 4 FDA inspections on record (1 OAI), 1 Form 483, last inspected April 11, 2019.

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## Details

- Name: Dermazone LLC
- FEI Number: 1000113908
- Address Line 1: 2440 30th Ave N
- City: Saint Petersburg
- State: Florida
- Zip Code: 33713
- Country Name: United States
- Address: 2440 30th Ave N, Saint Petersburg, Florida 33713, United States
- Country: United States

## Related Documents

- [483 - Dermazone LLC - 2022-12-06](https://www.keypedia.com/records/483/dermazone-llc/47dedf82-e4ae-432c-bb17-98915a31435b) — source: FDA, date: December 6, 2022
- [483 - Dermazone LLC - 2019-04-11](https://www.keypedia.com/records/483/dermazone-llc/0dfb36de-04ff-4036-a0fe-683d4018d87b) — source: FDA, date: April 11, 2019
- FDA Inspection 1086039 - Dermazone LLC - 2019-04-11 — classification: No Action Indicated (NAI), source: FDA, date: April 11, 2019
- [FDA Inspection 1086039 - Dermazone LLC - 2019-04-11](https://www.keypedia.com/records/fda_inspections/dermazone-llc/676e6519-f0e4-444d-9874-8c50f117ee67) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 11, 2019
- [FDA Inspection 951835 - Dermazone LLC - 2015-11-24](https://www.keypedia.com/records/fda_inspections/dermazone-llc/ae0dfb6b-6863-46df-b29e-a62095ba98c3) — classification: Official Action Indicated (OAI), source: FDA, date: November 24, 2015
- FDA Inspection 806119 - Dermazone LLC - 2012-11-01 — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2012
- FDA Inspection 806119 - Dermazone LLC - 2012-11-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 1, 2012
- [FDA Inspection 544410 - Dermazone LLC - 2008-11-05](https://www.keypedia.com/records/fda_inspections/dermazone-llc/13f966de-76a8-4b85-90e3-f48e30439d6d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 5, 2008

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