# Anda, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/anda-inc/04dd141d-a873-47e0-874f-9745eb88ee59

> Inspection records and compliance data for Anda, Inc. in Weston, Florida. Access full analysis and detailed observations.

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## Details

- Name: Anda, Inc.
- FEI Number: 3004024951
- City: Weston
- State: Florida
- Country Name: United States
- Address Line 1: 2915 Weston Rd
- Zip Code: 33331

## Related Documents

- [FDA Inspection 1282101 - Anda, Inc. - 2025-10-28](https://www.globalkeysolutions.net/records/fda_inspections/anda-inc/c1fa9e00-a81c-43f9-ad51-f948edd23542) — source: FDA, date: October 28, 2025
- [FDA Inspection 1044428 - Anda, Inc. - 2017-12-14](https://www.globalkeysolutions.net/records/fda_inspections/anda-inc/dabbafd1-af4d-486e-9e3c-92e77af165c3) — classification: No Action Indicated (NAI), source: FDA, date: December 14, 2017
- [FDA Inspection 1044428 - Anda, Inc. - 2017-12-14](https://www.globalkeysolutions.net/records/fda_inspections/anda-inc/bf8033a8-429c-4d62-8c60-86acec41a06f) — classification: No Action Indicated (NAI), source: FDA, date: December 14, 2017
- [FDA Inspection 1044428 - Anda, Inc. - 2017-12-14](https://www.globalkeysolutions.net/records/fda_inspections/anda-inc/7b2c5ead-48bc-4990-a703-db4b3af6b2ed) — classification: No Action Indicated (NAI), source: FDA, date: December 14, 2017
- [FDA Inspection 816772 - Anda, Inc. - 2013-01-10](https://www.globalkeysolutions.net/records/fda_inspections/anda-inc/0c6940a7-83f4-4a72-ae42-cd307d82c7ae) — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2013
- [FDA Inspection 816772 - Anda, Inc. - 2013-01-10](https://www.globalkeysolutions.net/records/fda_inspections/anda-inc/67f1421f-a90d-4048-8823-3d0a51de2f3c) — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2013
- [FDA Inspection 816772 - Anda, Inc. - 2013-01-10](https://www.globalkeysolutions.net/records/fda_inspections/anda-inc/8202c077-e76e-4128-a61c-e5ef7edf5da6) — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2013

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