Company
United StatesZimmer Biomet Mid Atlantic, Baltimore, MD – FDA Inspections
Inspection records and compliance data for Zimmer Biomet Mid Atlantic in Baltimore, Maryland. 2 FDA inspections on record, last inspected November 29, 2011.
Company Profile
This profile covers Zimmer Biomet Mid Atlantic based in Baltimore, Maryland, United States.
FDA Inspection History
- FDA inspections
- 2
- OAI
- 0
- VAI
- 0
- NAI
- 2
- Form 483s
- 0
- Warning letters
- 0
First inspected July 14, 2009. Last inspected November 29, 2011.
FDA inspections (2)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| November 29, 2011 | NAI | Biologics · Human Cellular, Tissue, and Gene Therapies | 756269 |
| July 14, 2009 | NAI | Biologics · Human Cellular, Tissue, and Gene Therapies | 596505 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Zimmer Biomet Mid Atlantic
FEI Number
3003834151
Address
9114 Philadelphia Rd Ste 100, Baltimore, Maryland 21237, United States
Country
United States
ID: 1cd1bb42-1242-4419-8505-3b1110a79207