FDA Inspection
EMSL Analytical, Inc. dba MPL LaboratoriesEMSL Analytical, Inc. dba MPL Laboratories – FDA Inspection, Sep 18, 2009
Record Details
This FDA Inspection record concerns EMSL Analytical, Inc. dba MPL Laboratories, with an inspection on September 18, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- September 18, 2009
- Product Type
- Drugs
View Company Profile
ID · af70fe70-b203-4422-b1a2-a0e2a867b6e5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 611938
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.160(a)Deviations from laboratory control requirements
- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.194(a)(8)Second person sign off
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of EMSL Analytical, Inc. dba MPL Laboratories
6| Date | Classification | Office | Project area |
|---|---|---|---|
| May 21, 2026 | Not classified | New Jersey District Office | Drug Quality Assurance |
| January 12, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 3, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 5, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 9, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for EMSL Analytical, Inc. dba MPL Laboratories
- FDA Inspection 1318220 - 2026-05-21
- FDA Inspection 1227791 - 2024-01-12
- FDA Inspection 989130 - 2016-10-03
- FDA Inspection 894261 - 2014-09-05
- FDA Inspection 756470 - 2011-12-09
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