# Provimi de Puerto Rico, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/provimi-de-puerto-rico-inc/4d49214a-4c2d-4f5d-8cf2-581671a67c8c

> Inspection records and compliance data for Provimi de Puerto Rico, Inc. in Morovis, Puerto Rico. Access full analysis and detailed observations.

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## Details

- Name: Provimi de Puerto Rico, Inc.
- FEI Number: 3004302089
- City: Morovis
- State: Puerto Rico
- Country Name: United States
- Address Line 1: Carr. 634, Km 5.5, Bo. Franquez
- Zip Code: 00687

## Related Documents

- [FDA Inspection 1268853 - Provimi de Puerto Rico, Inc. - 2025-04-25](https://www.globalkeysolutions.net/records/fda_inspections/provimi-de-puerto-rico-inc/2aea1a86-908f-4a78-9c00-79e032d5bbef) — source: FDA, date: April 25, 2025
- [FDA Inspection 1268853 - Provimi de Puerto Rico, Inc. - 2025-04-25](https://www.globalkeysolutions.net/records/fda_inspections/provimi-de-puerto-rico-inc/fd63df35-4d8f-4a04-99b1-0764c44475fc) — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2025
- [FDA Inspection 1268853 - Provimi de Puerto Rico, Inc. - 2025-04-25](https://www.globalkeysolutions.net/records/fda_inspections/provimi-de-puerto-rico-inc/085386ab-006d-4d57-9f6d-694529f7aca0) — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2025
- [FDA Inspection 1036341 - Provimi de Puerto Rico, Inc. - 2017-12-29](https://www.globalkeysolutions.net/records/fda_inspections/provimi-de-puerto-rico-inc/1bd56de7-7651-48b2-9779-b9e990aeae0f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 29, 2017
- [FDA Inspection 730080 - Provimi de Puerto Rico, Inc. - 2011-06-15](https://www.globalkeysolutions.net/records/fda_inspections/provimi-de-puerto-rico-inc/6623970a-3981-44e8-95f4-60cbdb2d5fe3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2011
- [FDA Inspection 730080 - Provimi de Puerto Rico, Inc. - 2011-06-15](https://www.globalkeysolutions.net/records/fda_inspections/provimi-de-puerto-rico-inc/81fd4023-c47d-4ef2-92f8-b678b1d9efc7) — classification: No Action Indicated (NAI), source: FDA, date: June 15, 2011

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