# PROLAC, INC., Bayamon, PR – FDA Inspections

Source: https://www.keypedia.com/companies/prolac-inc/4f233804-7168-46aa-bf76-d5aaea446e58

> Inspection records and compliance data for PROLAC, INC. in Bayamon, Puerto Rico. 4 FDA inspections on record (1 OAI), last inspected September 05, 2012.

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## Details

- Name: PROLAC, INC.
- FEI Number: 2619869
- Address Line 1: Calle Oeste 2 #15, Rio Plantation
- City: Bayamon
- State: Puerto Rico
- Zip Code: 00961
- Country Name: United States
- Address: Calle Oeste 2 #15, Rio Plantation, Bayamon, Puerto Rico 00961, United States
- Country: United States

## Related Documents

- FDA Inspection 797940 - PROLAC, INC. - 2012-09-05 — classification: No Action Indicated (NAI), source: FDA, date: September 5, 2012
- FDA Inspection 797940 - PROLAC, INC. - 2012-09-05 — classification: No Action Indicated (NAI), source: FDA, date: September 5, 2012
- FDA Inspection 723920 - PROLAC, INC. - 2011-05-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2011
- FDA Inspection 723920 - PROLAC, INC. - 2011-05-10 — classification: Official Action Indicated (OAI), source: FDA, date: May 10, 2011
- [FDA Inspection 723920 - PROLAC, INC. - 2011-05-10](https://www.keypedia.com/records/fda_inspections/prolac-inc/9207dd40-0808-43dd-a4f2-23a0b5ba1489) — classification: Official Action Indicated (OAI), source: FDA, date: May 10, 2011
- FDA Inspection 723920 - PROLAC, INC. - 2011-05-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2011
- FDA Inspection 677862 - PROLAC, INC. - 2010-09-09 — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2010
- FDA Inspection 677862 - PROLAC, INC. - 2010-09-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 9, 2010
- FDA Inspection 677862 - PROLAC, INC. - 2010-09-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 9, 2010
- FDA Inspection 612996 - PROLAC, INC. - 2009-09-21 — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2009

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