VitaCare Labs Inc.
FDA inspection history on file, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483.
Cited most
Across all VitaCare Labs observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
The complete VitaCare Labs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-05-16 | 483 Form 483 | — | 6 | $99 |
Investigators on these documents
FEI number 3008920776 · most recent document May 16, 2025
About VitaCare Labs Inc.
How many FDA Form 483s has VitaCare Labs Inc. received?
FDA Intel has 1 Form 483 on file for VitaCare Labs Inc.; the most recent is dated May 16, 2025.
When was VitaCare Labs Inc. last inspected by FDA?
The most recent FDA inspection document on file for VitaCare Labs Inc. is a Form 483 dated May 16, 2025.
What did FDA cite at VitaCare Labs Inc.?
The regulations cited most in the observations on file for VitaCare Labs Inc. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time.