Company
GermanyMueller-Omicron GmbH & Co. KG, Lindlar, Germany – FDA Inspections
Inspection records and compliance data for Mueller-Omicron GmbH & Co. KG in Lindlar. 1 FDA inspection on record, last inspected November 15, 2012.
Company Profile
This profile covers Mueller-Omicron GmbH & Co. KG based in Lindlar, Germany.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 1
- NAI
- 0
- Form 483s
- 0
- Warning letters
- 0
Inspected November 15, 2012.
Most cited issue areas
- Design changes - Lack of or Inadequate Procedures1 inspection
- Design output - Lack of or inadequate procedures1 inspection
- Design review - Lack of or inadequate procedures1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| November 15, 2012 | VAI | Medical Devices & Rad Health · Compliance: Devices | 809889 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Mueller-Omicron GmbH & Co. KG
FEI Number
3001550695
Address
Schlosserstr. 1, Lindlar, Germany
Country
Germany
ID: b9babde2-6840-4dd2-af85-0b9ea626818f