# FDA Inspection 1100788 - Protalix Ltd. - July 11, 2019

Source: https://www.keypedia.com/records/fda_inspections/protalix-ltd/8de2c344-4602-4db9-be98-cb4c02aa2028
Source feed: FDA_Inspections

> FDA Inspection 1100788 for Protalix Ltd. on July 11, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100788
- Company Name: Protalix Ltd.
- Inspection Date: 2019-07-11
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 931121 - 2015-05-14](https://www.keypedia.com/records/fda_inspections/protalix-ltd/abc84688-15b9-4228-9c66-7206f29b9777)
- [FDA Inspection 697924 - 2010-10-17](https://www.keypedia.com/records/fda_inspections/protalix-ltd/6aa6970e-06ad-4d7e-a129-938c58c4aa09)

Company: https://www.keypedia.com/companies/protalix-ltd/03315ab5-c1f4-41af-ab04-56c4658d1eeb

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c