# Ramar International Corporation, Pittsburg, CA – FDA Inspections

Source: https://www.keypedia.com/companies/ramar-international-corporation/450ff9c8-e8df-4f42-9903-826339154164

> Inspection records and compliance data for Ramar International Corporation in Pittsburg, California. 5 FDA inspections on record, 1 Form 483, last inspected March 07, 2022.

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## Details

- Name: Ramar International Corporation
- FEI Number: 3007492092
- Address Line 1: 335 Central Ave
- City: Pittsburg
- State: California
- Zip Code: 94565
- Country Name: United States
- Address: 335 Central Ave, Pittsburg, California 94565, United States
- Country: United States

## Related Documents

- FDA Inspection 1164831 - Ramar International Corporation - 2022-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2022
- FDA Inspection 1164831 - Ramar International Corporation - 2022-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2022
- [FDA Inspection 1020605 - Ramar International Corporation - 2017-07-27](https://www.keypedia.com/records/fda_inspections/ramar-international-corporation/f024ac81-020e-4017-8d1f-b10da2a49ca8) — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2017
- FDA Inspection 1020605 - Ramar International Corporation - 2017-07-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 27, 2017
- [FDA Inspection 984354 - Ramar International Corporation - 2016-05-10](https://www.keypedia.com/records/fda_inspections/ramar-international-corporation/aff6dbac-107d-4929-adee-7962bf89c2a9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2016
- FDA Inspection 720304 - Ramar International Corporation - 2011-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2011
- FDA Inspection 668012 - Ramar International Corporation - 2010-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010
- FDA Inspection 668012 - Ramar International Corporation - 2010-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2010

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