# Captek Softgel International - Inspection Records

Source: https://www.keypedia.com/companies/captek-softgel-international/c1401013-74f7-4417-afab-bf237af03606

> Inspection records and compliance data for Captek Softgel International in Vista, California. Access full analysis and detailed observations.

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## Details

- Name: Captek Softgel International
- FEI Number: 3001417109
- City: Vista
- State: California
- Country Name: United States
- Address Line 1: 2710 Progress St
- Zip Code: 92081
- Business Operations: FDF MANUFACTURE

## Related Documents

- [FDA Inspection 1116153 - Captek Softgel International - 2020-01-09](https://www.keypedia.com/records/fda_inspections/captek-softgel-international/3cafcad2-4afb-4b98-86e3-c243548b5fe8) — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2020
- [FDA Inspection 1008962 - Captek Softgel International - 2017-04-06](https://www.keypedia.com/records/fda_inspections/captek-softgel-international/4b609179-db2b-4c63-b267-8a90e07551f0) — classification: No Action Indicated (NAI), source: FDA, date: April 6, 2017
- [FDA Inspection 1008962 - Captek Softgel International - 2017-04-06](https://www.keypedia.com/records/fda_inspections/captek-softgel-international/e1726378-001d-4212-b045-9a61431c51b9) — classification: No Action Indicated (NAI), source: FDA, date: April 6, 2017
- [FDA Inspection 908973 - Captek Softgel International - 2015-01-06](https://www.keypedia.com/records/fda_inspections/captek-softgel-international/3a5ac2bf-c0b8-4309-8963-bff4e2e53fef) — classification: No Action Indicated (NAI), source: FDA, date: January 6, 2015
- [FDA Inspection 908973 - Captek Softgel International - 2015-01-06](https://www.keypedia.com/records/fda_inspections/captek-softgel-international/c5c05866-5ef8-4436-a333-e70d04ff0e63) — classification: No Action Indicated (NAI), source: FDA, date: January 6, 2015
- [FDA Inspection 736001 - Captek Softgel International - 2010-11-24](https://www.keypedia.com/records/fda_inspections/captek-softgel-international/cd2fb691-7085-4ea9-9005-4bc7163b87c9) — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2010

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