# Clinica de Fertlidad HIMA San Pablo Caguas, Caguas, PR – FDA Inspections

Source: https://www.keypedia.com/companies/clinica-de-fertlidad-hima-san-pablo-caguas/df99a310-b3bb-44db-9e23-17a46ffcebc0

> Inspection records and compliance data for Clinica de Fertlidad HIMA San Pablo Caguas in Caguas, Puerto Rico. 5 FDA inspections on record, last inspected November 15, 2023.

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## Details

- Name: Clinica de Fertlidad HIMA San Pablo Caguas
- FEI Number: 3006043758
- Address Line 1: Munoz Rivera Avenue A-1 Suite 303
- City: Caguas
- State: Puerto Rico
- Zip Code: 00725
- Country Name: United States
- Address: Munoz Rivera Avenue A-1 Suite 303, Caguas, Puerto Rico 00725, United States
- Country: United States

## Related Documents

- FDA Inspection 1223851 - Clinica de Fertlidad HIMA San Pablo Caguas - 2023-11-15 — classification: No Action Indicated (NAI), source: FDA, date: November 15, 2023
- [FDA Inspection 1174338 - Clinica de Fertlidad HIMA San Pablo Caguas - 2022-07-05](https://www.keypedia.com/records/fda_inspections/clinica-de-fertlidad-hima-san-pablo-caguas/7765e7dc-7bff-4120-95db-58ea423661ae) — classification: No Action Indicated (NAI), source: FDA, date: July 5, 2022
- FDA Inspection 1174338 - Clinica de Fertlidad HIMA San Pablo Caguas - 2022-07-05 — classification: No Action Indicated (NAI), source: FDA, date: July 5, 2022
- FDA Inspection 1051837 - Clinica de Fertlidad HIMA San Pablo Caguas - 2018-04-30 — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2018
- [FDA Inspection 1051837 - Clinica de Fertlidad HIMA San Pablo Caguas - 2018-04-30](https://www.keypedia.com/records/fda_inspections/clinica-de-fertlidad-hima-san-pablo-caguas/f7aaecc0-74c7-4304-b6d3-bcfe66cccec5) — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2018
- FDA Inspection 967752 - Clinica de Fertlidad HIMA San Pablo Caguas - 2016-01-26 — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2016
- FDA Inspection 815348 - Clinica de Fertlidad HIMA San Pablo Caguas - 2012-11-30 — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2012

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