# Procaps Laboratories Inc., Henderson, NV – FDA Inspections

Source: https://www.keypedia.com/companies/procaps-laboratories-inc/2e08e093-78a0-4b5f-a73c-da967807cc34

> Inspection records and compliance data for Procaps Laboratories Inc. in Henderson, Nevada. 5 FDA inspections on record, 1 Form 483, last inspected September 12, 2025.

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## Details

- Name: Procaps Laboratories Inc.
- FEI Number: 3003902875
- Address Line 1: 430 Parkson Rd
- City: Henderson
- State: Nevada
- Zip Code: 89011
- Country Name: United States
- Address: 430 Parkson Rd, Henderson, Nevada 89011, United States
- Country: United States

## Related Documents

- FDA Inspection 1286914 - Procaps Laboratories Inc. - 2025-09-12 — source: FDA, date: September 12, 2025
- FDA Inspection 1286914 - Procaps Laboratories Inc. - 2025-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2025
- FDA Inspection 1174350 - Procaps Laboratories Inc. - 2022-06-22 — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2022
- [FDA Inspection 1077716 - Procaps Laboratories Inc. - 2018-11-09](https://www.keypedia.com/records/fda_inspections/procaps-laboratories-inc/9c13610b-2530-48e7-937e-51b04fb57230) — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2018
- FDA Inspection 1077716 - Procaps Laboratories Inc. - 2018-11-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 9, 2018
- [FDA Inspection 973843 - Procaps Laboratories Inc. - 2016-03-08](https://www.keypedia.com/records/fda_inspections/procaps-laboratories-inc/d834718c-f7c0-4f11-9b91-7aff2a9c4b21) — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2016
- FDA Inspection 973843 - Procaps Laboratories Inc. - 2016-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2016
- [FDA Inspection 936412 - Procaps Laboratories Inc. - 2015-07-29](https://www.keypedia.com/records/fda_inspections/procaps-laboratories-inc/bb6f97dc-6407-43d8-8564-6f27ba76cdc0) — classification: No Action Indicated (NAI), source: FDA, date: July 29, 2015

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