# Panaderia Y Reposteria La Moderna, Moca, PR – FDA Inspections

Source: https://www.keypedia.com/companies/panaderia-y-reposteria-la-moderna/3ddfeb14-b70b-4e4b-9167-32ec5031c87a

> Inspection records and compliance data for Panaderia Y Reposteria La Moderna in Moca, Puerto Rico. 7 FDA inspections on record, last inspected July 01, 2026.

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## Details

- Name: Panaderia Y Reposteria La Moderna
- FEI Number: 3005147771
- Address Line 1: 369 Calle Jose C Barbosa
- City: Moca
- State: Puerto Rico
- Zip Code: 00676
- Country Name: United States
- Address: 369 Calle Jose C Barbosa, Moca, Puerto Rico 00676, United States
- Country: United States

## Related Documents

- FDA Inspection 1291287 - Panaderia Y Reposteria La Moderna - 2026-07-01 — source: FDA, date: July 1, 2026
- FDA Inspection 1247703 - Panaderia Y Reposteria La Moderna - 2024-08-19 — source: FDA, date: August 19, 2024
- FDA Inspection 1159827 - Panaderia Y Reposteria La Moderna - 2021-12-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 30, 2021
- FDA Inspection 1159827 - Panaderia Y Reposteria La Moderna - 2021-12-30 — classification: No Action Indicated (NAI), source: FDA, date: December 30, 2021
- FDA Inspection 1058866 - Panaderia Y Reposteria La Moderna - 2018-06-06 — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2018
- [FDA Inspection 940715 - Panaderia Y Reposteria La Moderna - 2015-09-04](https://www.keypedia.com/records/fda_inspections/panaderia-y-reposteria-la-moderna/c1295daf-f33b-4127-8bb9-6e089778cae6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 4, 2015
- FDA Inspection 804639 - Panaderia Y Reposteria La Moderna - 2012-10-24 — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2012
- FDA Inspection 804639 - Panaderia Y Reposteria La Moderna - 2012-10-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 24, 2012
- FDA Inspection 666834 - Panaderia Y Reposteria La Moderna - 2010-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010

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