# FDA Inspection 658222 - Biomat USA, Inc. DBA Grifols PlasmaCare, Inc. - April 08, 2010

Source: https://www.keypedia.com/records/fda_inspections/biomat-usa-inc-dba-grifols-plasmacare-inc/e0617a4e-9970-4425-aa2e-65b475098623
Source feed: FDA_Inspections

> FDA Inspection 658222 for Biomat USA, Inc. DBA Grifols PlasmaCare, Inc. on April 08, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 658222
- Company Name: Biomat USA, Inc. DBA Grifols PlasmaCare, Inc.
- Inspection Date: 2010-04-08
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

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Company: https://www.keypedia.com/companies/biomat-usa-inc-dba-grifols-plasmacare-inc/7ffb9728-73eb-4e4b-b8db-995e6532e794

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