# FDA Inspection 543569 - Biograft de Mexico - October 01, 2008

Source: https://www.keypedia.com/records/fda_inspections/biograft-de-mexico/7cad7dc8-a902-4e08-9275-466b4dfe7651
Source feed: FDA_Inspections

> FDA Inspection 543569 for Biograft de Mexico on October 01, 2008. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 543569
- Company Name: Biograft de Mexico
- Inspection Date: 2008-10-01
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

Company: https://www.keypedia.com/companies/biograft-de-mexico/d424cc4d-6559-4cbd-b2b3-e5703f5c7207

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d