# A. Ochoa Dist & Mfg., LLC - Inspection Records

Source: https://www.keypedia.com/companies/a-ochoa-dist-mfg-llc/63544c48-0251-4d46-bf1b-632950ec1ab5

> Inspection records and compliance data for A. Ochoa Dist & Mfg., LLC in Barceloneta, Puerto Rico. Access full analysis and detailed observations.

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## Details

- Name: A. Ochoa Dist & Mfg., LLC
- FEI Number: 3012238370
- City: Barceloneta
- State: Puerto Rico
- Country Name: United States
- Address Line 1: Calle 14 # 2 Bo. Tiburones
- Zip Code: 00617

## Related Documents

- [FDA Inspection 1193414 - A. Ochoa Dist & Mfg., LLC - 2022-12-20](https://www.keypedia.com/records/fda_inspections/a-ochoa-dist-mfg-llc/2006f009-5ecb-44a7-ae15-47a2168b6f6a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 20, 2022
- [FDA Inspection 1096688 - A. Ochoa Dist & Mfg., LLC - 2019-04-24](https://www.keypedia.com/records/fda_inspections/a-ochoa-dist-mfg-llc/0d283ec0-a562-4d16-89c2-a5d4445c47cf) — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2019
- [FDA Inspection 1010937 - A. Ochoa Dist & Mfg., LLC - 2017-05-16](https://www.keypedia.com/records/fda_inspections/a-ochoa-dist-mfg-llc/3c68927e-df42-4fd0-9e00-ec881844ee93) — classification: No Action Indicated (NAI), source: FDA, date: May 16, 2017
- [FDA Inspection 913414 - A. Ochoa Dist & Mfg., LLC - 2015-02-10](https://www.keypedia.com/records/fda_inspections/a-ochoa-dist-mfg-llc/b8ee01d0-25c1-4540-a33d-afba8a22af9d) — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2015
- [FDA Inspection 745009 - A. Ochoa Dist & Mfg., LLC - 2011-09-16](https://www.keypedia.com/records/fda_inspections/a-ochoa-dist-mfg-llc/f9b6d039-ec21-4da6-9b01-09990297b845) — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2011
- [FDA Inspection 559373 - A. Ochoa Dist & Mfg., LLC - 2009-02-02](https://www.keypedia.com/records/fda_inspections/a-ochoa-dist-mfg-llc/438e9ca9-4b95-48f7-9e16-b1917515b3b0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 2, 2009

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