# FDA Inspection 984810 - Biomat USA, Inc. DBA Grifols PlasmaCare, Inc. - September 09, 2016

Source: https://www.keypedia.com/records/fda_inspections/biomat-usa-inc-dba-grifols-plasmacare-inc/4bedcd6d-3cde-47d9-855b-e30341e0b7b9
Source feed: FDA_Inspections

> FDA Inspection 984810 for Biomat USA, Inc. DBA Grifols PlasmaCare, Inc. on September 09, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 984810
- Company Name: Biomat USA, Inc. DBA Grifols PlasmaCare, Inc.
- Inspection Date: 2016-09-09
- Classification: Voluntary Action Indicated (VAI)
- 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