# Grifols Bio Supplies Inc., Baltimore, MD – FDA Inspections

Source: https://www.keypedia.com/companies/grifols-bio-supplies-inc/0a7e2dcf-e4f6-47c8-94aa-96bca2201b43

> Inspection records and compliance data for Grifols Bio Supplies Inc. in Baltimore, Maryland. 7 FDA inspections on record, last inspected June 28, 2022.

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## Details

- Name: Grifols Bio Supplies Inc.
- FEI Number: 1177773
- Address Line 1: Dba Maryland Biological Services, 6651 Belair Rd
- City: Baltimore
- State: Maryland
- Zip Code: 21206
- Country Name: United States
- Address: Dba Maryland Biological Services, 6651 Belair Rd, Baltimore, Maryland 21206, United States
- Country: United States

## Related Documents

- FDA Inspection 1173907 - Grifols Bio Supplies Inc. - 2022-06-28 — classification: No Action Indicated (NAI), source: FDA, date: June 28, 2022
- FDA Inspection 1173907 - Grifols Bio Supplies Inc. - 2022-06-28 — classification: No Action Indicated (NAI), source: FDA, date: June 28, 2022
- FDA Inspection 1080666 - Grifols Bio Supplies Inc. - 2019-01-18 — classification: No Action Indicated (NAI), source: FDA, date: January 18, 2019
- FDA Inspection 1022920 - Grifols Bio Supplies Inc. - 2017-07-20 — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2017
- FDA Inspection 932350 - Grifols Bio Supplies Inc. - 2015-07-02 — classification: No Action Indicated (NAI), source: FDA, date: July 2, 2015
- FDA Inspection 854893 - Grifols Bio Supplies Inc. - 2013-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2013
- [FDA Inspection 774262 - Grifols Bio Supplies Inc. - 2012-04-02](https://www.keypedia.com/records/fda_inspections/grifols-bio-supplies-inc/291ce2d8-70ce-43b3-8b4b-5a3d7b54e038) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 2, 2012
- [FDA Inspection 663574 - Grifols Bio Supplies Inc. - 2010-05-18](https://www.keypedia.com/records/fda_inspections/grifols-bio-supplies-inc/5acb484b-054b-460d-9089-0182baa71c13) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 18, 2010

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