# Pedicraft, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/pedicraft-inc/348fce14-ecf0-487a-9b55-1d1d07357e2a

> Inspection records and compliance data for Pedicraft, Inc. in Jacksonville, Florida. Access full analysis and detailed observations.

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## Details

- Name: Pedicraft, Inc.
- FEI Number: 1043568
- City: Jacksonville
- State: Florida
- Country Name: United States
- Address Line 1: 4134 Saint Augustine Rd
- Zip Code: 32207

## Related Documents

- [483 - Pedicraft, Inc. - 2025-07-25](https://www.keypedia.com/records/483/pedicraft-inc/ebcf6cef-37b6-4c63-815f-f14be00cb9c0) — source: FDA, date: July 25, 2025
- [FDA Inspection 1276546 - Pedicraft, Inc. - 2025-07-25](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/425e8644-39ec-4ebe-b7cd-209c2d0dd654) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 25, 2025
- [FDA Inspection 1276546 - Pedicraft, Inc. - 2025-07-25](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/4e12d48e-0eeb-4111-aa1f-a96f6e2d7862) — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2025
- [FDA Inspection 1276546 - Pedicraft, Inc. - 2025-07-25](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/e88c978a-17fd-4694-b194-d1b04ce4c553) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 25, 2025
- [FDA Inspection 1276546 - Pedicraft, Inc. - 2025-07-25](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/5770caf1-56c6-45ec-bbd5-8ed6109d05d1) — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2025
- [483 - Pedicraft, Inc. - 2020-01-17](https://www.keypedia.com/records/483/pedicraft-inc/6e8fab6e-c663-4a15-bebb-c846af072283) — source: FDA, date: January 17, 2020
- [FDA Inspection 1115473 - Pedicraft, Inc. - 2020-01-17](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/6b7e38d7-c322-40e2-ac91-aa8ab12e90a7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 17, 2020
- [FDA Inspection 1115473 - Pedicraft, Inc. - 2020-01-17](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/e386b222-7742-4fa0-bb4e-529aba61298a) — classification: No Action Indicated (NAI), source: FDA, date: January 17, 2020
- [FDA Inspection 992413 - Pedicraft, Inc. - 2016-10-19](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/408754a7-acb3-4fc0-a6fb-082541709572) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 19, 2016
- [FDA Inspection 992413 - Pedicraft, Inc. - 2016-10-19](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/1c76e912-452a-445b-88a8-6bb7a5082f90) — classification: No Action Indicated (NAI), source: FDA, date: October 19, 2016
- [FDA Inspection 878550 - Pedicraft, Inc. - 2014-04-25](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/8b5ff560-6c5b-45dd-96e4-a60fc28f9b99) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 25, 2014
- [FDA Inspection 878550 - Pedicraft, Inc. - 2014-04-25](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/583c19b2-2943-4540-b1ce-30f0a81e2930) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 25, 2014

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