# Mendez & Co., Inc., Guaynabo, PR – FDA Inspections

Source: https://www.keypedia.com/companies/mendez-co-inc/9bd572e0-950f-4dba-a1f2-7327f7012399

> Inspection records and compliance data for Mendez & Co., Inc. in Guaynabo, Puerto Rico. 7 FDA inspections on record, 2 Form 483s, last inspected September 26, 2022.

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## Details

- Name: Mendez & Co., Inc.
- FEI Number: 3011572191
- Address Line 1: Expreso Martinez Nadal, Carr #20 Km 2.4 Marginal Este
- City: Guaynabo
- State: Puerto Rico
- Zip Code: 00969
- Country Name: United States
- Address: Expreso Martinez Nadal, Carr #20 Km 2.4 Marginal Este, Guaynabo, Puerto Rico 00969, United States
- Country: United States

## Related Documents

- FDA Inspection 1181311 - Mendez & Co., Inc. - 2022-09-26 — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2022
- FDA Inspection 1181311 - Mendez & Co., Inc. - 2022-09-26 — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2022
- FDA Inspection 1120280 - Mendez & Co., Inc. - 2020-02-27 — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2020
- [FDA Inspection 1094837 - Mendez & Co., Inc. - 2019-06-24](https://www.keypedia.com/records/fda_inspections/mendez-co-inc/f4c70dd5-f7bf-4bfe-a966-f746c13faf31) — source: FDA, date: June 24, 2019
- [FDA Inspection 1059716 - Mendez & Co., Inc. - 2018-07-20](https://www.keypedia.com/records/fda_inspections/mendez-co-inc/a92aff4f-4213-4f82-b993-f84a81270c04) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 20, 2018
- FDA Inspection 976733 - Mendez & Co., Inc. - 2016-05-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 19, 2016
- [FDA Inspection 976995 - Mendez & Co., Inc. - 2016-03-15](https://www.keypedia.com/records/fda_inspections/mendez-co-inc/63a19407-261b-4df7-b631-86823e61bbfb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 15, 2016
- FDA Inspection 817507 - Mendez & Co., Inc. - 2012-08-27 — classification: No Action Indicated (NAI), source: FDA, date: August 27, 2012

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